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  • Journals  (66)
  • Articles  (208,231)
  • Oxford University Press  (208,297)
  • Biology  (208,297)
Collection
  • Journals  (66)
  • Articles  (208,231)
Years
Media Type
  • 1
    Journal cover
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    Oxford University Press
    Online: 1(1).2016 –
    Publisher: Oxford University Press
    Electronic ISSN: 2397-7000
    Topics: Biology
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  • 2
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    Oxford University Press | HighWire Press
    Online: 37(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0032-0781
    Electronic ISSN: 1471-9053
    Topics: Biology
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  • 3
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    Oxford University Press
    Online: 1(1).2013 –
    Publisher: Oxford University Press
    Electronic ISSN: 2051-1434
    Topics: Biology
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  • 4
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 1(1).1969 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Print ISSN: 0024-4066
    Electronic ISSN: 1095-8312
    Topics: Biology
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  • 5
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    Oxford University Press | Society for the Study of Reproduction, BioOne
    Online: 54(1).1996 –
    Publisher: Oxford University Press , Society for the Study of Reproduction, BioOne
    Print ISSN: 0006-3363
    Electronic ISSN: 1529-7268
    Topics: Biology , Medicine
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  • 6
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    Oxford University Press
    Online: 12.1996 – (older than 12 months)
    Publisher: Oxford University Press
    Print ISSN: 1367-4803
    Electronic ISSN: 1367-4811 , 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 7
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    Oxford University Press | HighWire Press
    Online: 1(1).2000 – (older than 24 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1465-4644
    Electronic ISSN: 1468-4357
    Topics: Biology , Mathematics , Medicine
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  • 8
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    Oxford University Press
    Online: 1(1).2016 –
    Publisher: Oxford University Press
    Electronic ISSN: 2396-8923
    Topics: Biology
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  • 9
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    Oxford University Press | HighWire Press
    Online: 1(1).2000 – (older than 24 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1467-5463
    Electronic ISSN: 1477-4054
    Topics: Biology , Computer Science
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  • 10
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    Oxford University Press | HighWire Press
    Online: 1(1).2002 – (older than 24 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1473-9550 , 2041-2649
    Electronic ISSN: 1477-4062 , 2041-2647
    Topics: Biology , Chemistry and Pharmacology
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  • 11
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    Oxford University Press | HighWire Press
    Online: 1(1).2002 –
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1473-9550 , 2041-2649
    Electronic ISSN: 1477-4062 , 2041-2657
    Topics: Biology , Chemistry and Pharmacology
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  • 12
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier / Academic Press
    Online: 1(1).1856 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier / Academic Press
    Print ISSN: 0024-4074
    Electronic ISSN: 1095-8339
    Topics: Biology
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  • 13
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    Oxford University Press
    Online: 55.2009 –
    Publisher: Oxford University Press
    Print ISSN: 1674-5507
    Electronic ISSN: 2396-9814
    Topics: Biology
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  • 14
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    Oxford University Press
    Online: 2009 –
    Publisher: Oxford University Press
    Electronic ISSN: 1758-0463
    Topics: Biology
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  • 15
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 1.1985 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 0168-6445
    Electronic ISSN: 1574-6976
    Topics: Biology
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  • 16
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    Oxford University Press | HighWire Press
    Online: 5.1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0964-6906
    Electronic ISSN: 1460-2083
    Topics: Biology , Medicine
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  • 17
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    Oxford University Press | früher: Institute for Laboratory Animal Research (ILAR)
    Online: 31(1).1989 –
    Publisher: Oxford University Press , früher: Institute for Laboratory Animal Research (ILAR)
    Print ISSN: 0018-9960 , 1084-2020
    Electronic ISSN: 1930-6180
    Topics: Biology , Medicine
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  • 18
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    Oxford University Press | HighWire Press | International Council for the Exploration of the Seas (ICES)
    Online: 53.1996 –
    Formerly as: Journal du Conseil / Conseil Permanent International pour l'Exploration de la Mer (1926-1990) ; Publications de circonstance / Conseil Permanent International pour l'Exploration de la Mer  (1903–1926)
    Publisher: Oxford University Press , HighWire Press , International Council for the Exploration of the Seas (ICES)
    Corporation: International Council for the Exploration of the Sea, ICES
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
    Topics: Biology , Geosciences , Physics
    Abbreviation: ICES J Mar Sci
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  • 19
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    Oxford University Press
    Online: 1(1).2019 –
    Publisher: Oxford University Press
    Electronic ISSN: 2517-5025
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
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  • 20
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    Oxford University Press | HighWire Press
    Online: 1(1).1961 – (older than 12 months)
    Formerly as: American Zoologist  (1961–2001)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0003-1569 , 1540-7063
    Electronic ISSN: 1557-7023
    Topics: Biology
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  • 21
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    Oxford University Press | HighWire Press | International Council for the Exploration of the Seas (ICES)
    Online: 53(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press , International Council for the Exploration of the Seas (ICES)
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
    Topics: Biology , Geosciences , Physics
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  • 22
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    Oxford University Press | HighWire Press
    Online: 47(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0022-0957
    Electronic ISSN: 1460-2431
    Topics: Biology
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  • 23
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    Oxford University Press | HighWire Press
    Online: 62(1).1996 – (older than 12 months)
    Formerly as: Proceedings of the Malacological Society of London  (1893–1974)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0260-1230
    Electronic ISSN: 1464-3766
    Topics: Biology
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  • 24
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    Oxford University Press | früher SpringerNature
    Online: 1(1).1986 –
    Publisher: Oxford University Press , früher SpringerNature
    Print ISSN: 0169-4146 , 1367-5435
    Electronic ISSN: 1476-5535
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
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  • 25
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    Oxford University Press
    Online: 1(1).2009 – 11(12).2019
    Online: 1.2009 –
    Publisher: Oxford University Press
    Print ISSN: 1674-2788
    Electronic ISSN: 1673-520X , 1759-4685
    Topics: Biology
    Keywords: Zellbiologie
    Acronym: JMCB
    Abbreviation: J Mol Cell Biol
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  • 26
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    Entomological Society of America | Oxford University Press | BioOne
    Online: 1.2001 –
    Publisher: Entomological Society of America , Oxford University Press , BioOne
    Electronic ISSN: 1536-2442
    Topics: Biology
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  • 27
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    Oxford University Press
    Online: 1.2009 –
    Publisher: Oxford University Press
    Print ISSN: 1674-2788
    Electronic ISSN: 1673-520X , 1759-4685
    Topics: Biology
    Acronym: JMCB
    Abbreviation: J Mol Cell Biol
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  • 28
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    Oxford University Press
    Online: 18(1).1996 – (older than 12 months)
    Publisher: Oxford University Press
    Print ISSN: 0142-7873
    Electronic ISSN: 1464-3774
    Topics: Biology
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  • 29
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    Oxford University Press
    Online: 1.2012 –
    Publisher: Oxford University Press
    Electronic ISSN: 2047-217X
    Topics: Biology , Medicine
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  • 30
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    Oxford University Press | HighWire Press
    Online: 6(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0959-6658
    Electronic ISSN: 1460-2423
    Topics: Biology , Medicine
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  • 31
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    Oxford University Press | British Society for Antimicrobial Chemotherapy
    Online: 1(1).2019 –
    Publisher: Oxford University Press , British Society for Antimicrobial Chemotherapy
    Electronic ISSN: 2632-1823
    Topics: Biology
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  • 32
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    Oxford University Press | HighWire Press
    Online: 1.2009 –
    Publisher: Oxford University Press , HighWire Press
    Electronic ISSN: 1759-6653
    Topics: Biology
    Acronym: GBE
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  • 33
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    Oxford University Press | Entomological Society of America; BioOne
    Online: 1(1).1972 –
    Publisher: Oxford University Press , Entomological Society of America; BioOne
    Print ISSN: 0046-225X , 0046-2268
    Electronic ISSN: 1938-2936
    Topics: Biology
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  • 34
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 1.1977 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 0378-1097
    Electronic ISSN: 1574-6968
    Topics: Biology
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  • 35
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 1.2001 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 1567-1356
    Electronic ISSN: 1567-1364
    Topics: Biology
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  • 36
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 1.1985 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 0168-6496
    Electronic ISSN: 1574-6941
    Topics: Biology
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  • 37
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    Oxford University Press | Crustacean Society | BioOne
    Online: 1.1981 –
    Publisher: Oxford University Press , Crustacean Society , BioOne
    Print ISSN: 0278-0372
    Electronic ISSN: 1937-240X
    Topics: Biology
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  • 38
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    Oxford University Press | Entomological Society of America | BioOne
    Online: 1.1908 –
    Publisher: Oxford University Press , Entomological Society of America , BioOne
    Print ISSN: 0022-0493
    Electronic ISSN: 1938-291X
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
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  • 39
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    Entomological Society of America; BioOne | Oxford University Press
    Online: 1(1).1964 –
    Publisher: Entomological Society of America; BioOne , Oxford University Press
    Corporation: Entomological Society of America
    Print ISSN: 0022-2585
    Electronic ISSN: 1938-2928
    Topics: Biology
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  • 40
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    Oxford University Press | American Society of Mammalogists; BioOne
    Online: 1(1).1919 –
    Publisher: Oxford University Press , American Society of Mammalogists; BioOne
    Corporation: American Society of Mammalogists
    Print ISSN: 0022-2372
    Electronic ISSN: 1545-1542
    Topics: Biology
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  • 41
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    Oxford University Press
    Online: 1(1).1988 – (older than 24 months)
    Formerly as: FEMS Immunology and Medical Microbiology  (1993–2012)
    Publisher: Oxford University Press
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 0928-8244
    Electronic ISSN: 1574-695X , 2049-632X
    Topics: Biology
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  • 42
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    Oxford University Press | HighWire Press
    Online: 1(1).2008 –
    Publisher: Oxford University Press , HighWire Press
    Electronic ISSN: 1754-7431
    Topics: Biology
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  • 43
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    Oxford University Press | HighWire Press
    Online: 1(1).2000 –
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1467-5463
    Electronic ISSN: 1477-4054
    Topics: Biology , Computer Science
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  • 44
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier
    Online: 6.1993 –
    Formerly as: FEMS Immunology and Medical Microbiology  (1993–2012)
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier
    Corporation: Federation of European Microbiological Societies, FEMS
    Print ISSN: 0928-8244
    Electronic ISSN: 1574-695X , 2049-632X
    Topics: Biology , Medicine
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  • 45
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    Oxford University Press | HighWire Press
    Online: 7(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 1045-2249
    Electronic ISSN: 1465-7279
    Topics: Biology
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  • 46
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    The Entomological Society of America | Oxford University Press
    Online: 47(1).2001 – (older than 24 months)
    Publisher: The Entomological Society of America , Oxford University Press
    Print ISSN: 1046-2821
    Electronic ISSN: 2155-9902
    Topics: Biology
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  • 47
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    The Entomological Society of America | Oxford University Press
    Online: 36(1).1990 –
    Publisher: The Entomological Society of America , Oxford University Press
    Corporation: Entomological Society of America, ESA
    Print ISSN: 1046-2821
    Electronic ISSN: 2155-9902
    Topics: Biology
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  • 48
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    Entomological Society of America | BioOne | Oxford University Press
    Online: 1(1).1908 –
    Publisher: Entomological Society of America , BioOne , Oxford University Press
    Corporation: Entomological Society of America
    Print ISSN: 0013-8746
    Electronic ISSN: 1938-2901
    Topics: Biology
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  • 49
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    Oxford University Press | American Ornithologists Union
    Online: 113.1996 – (older than 24 months)
    Publisher: Oxford University Press , American Ornithologists Union
    Print ISSN: 0004-8038
    Electronic ISSN: 1938-4254
    Topics: Biology
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  • 50
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    Oxford University Press
    Online: 2009 –
    Publisher: Oxford University Press
    Electronic ISSN: 2041-2851
    Topics: Biology
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  • 51
    Journal cover
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    Oxford University Press | Entomological Society of America
    Online: 1.1976 –
    Publisher: Oxford University Press , Entomological Society of America
    Print ISSN: 0276-3656
    Electronic ISSN: 2155-9856
    Topics: Biology
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  • 52
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    Oxford University Press | HighWire Press
    Online: 71(1).1993 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0305-7364
    Electronic ISSN: 1095-8290
    Topics: Biology
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  • 53
    Journal cover
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    Oxford University Press | American Ornithologists Union | BioOne | JSTOR
    Online: 1.1996 –
    Publisher: Oxford University Press , American Ornithologists Union , BioOne , JSTOR
    Corporation: American Ornithologists
    Print ISSN: 0004-8038
    Electronic ISSN: 1938-4254
    Topics: Biology
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  • 54
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    Oxford University Press | HighWire Press
    Online: 87.1996 –
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0022-1503
    Electronic ISSN: 1465-7333
    Topics: Biology
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  • 55
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    Oxford University Press
    Online: 1(1).2008 – (older than 12 months)
    Publisher: Oxford University Press
    Print ISSN: 1752-9921
    Electronic ISSN: 1752-993X
    Topics: Biology
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  • 56
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    Oxford University Press
    Online: 1(1).2008 –
    Publisher: Oxford University Press
    Print ISSN: 1752-9921
    Electronic ISSN: 1752-993X
    Topics: Biology
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  • 57
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    Oxford University Press | Royal Society of Chemistry
    Online: 1.2009 – 7.2015
    Publisher: Oxford University Press , Royal Society of Chemistry
    Print ISSN: 1756-5901
    Electronic ISSN: 1756-591X
    Topics: Biology , Chemistry and Pharmacology
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  • 58
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    Oxford University Press
    Online: 1(1).2020 –
    Publisher: Oxford University Press
    Electronic ISSN: 2633-6685
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Medicine
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  • 59
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    Oxford University Press | American Society of Mammalogists; früher: BioOne
    Online: 1(1).1969 –
    Publisher: Oxford University Press , American Society of Mammalogists; früher: BioOne
    Corporation: American Society of Mammalogists
    Print ISSN: 0076-3519
    Electronic ISSN: 1545-1410
    Topics: Biology
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  • 60
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    Oxford University Press
    Online: 1(1).2019 –
    Publisher: Oxford University Press
    Electronic ISSN: 2631-9268
    Topics: Biology , Computer Science
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  • 61
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    Oxford University Press | HighWire Press
    Online: 11(1).1996 – (older than 12 months)
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0267-8357
    Electronic ISSN: 1464-3804
    Topics: Biology , Medicine
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  • 62
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    Oxford University Press
    Online: 1(1).2020 –
    Publisher: Oxford University Press
    Electronic ISSN: 2633-6693
    Topics: Biology
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  • 63
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    Oxford University Press | formerly: Wiley-Blackwell
    Online: 1(1).1942 –
    Publisher: Oxford University Press , formerly: Wiley-Blackwell
    Print ISSN: 0029-6643
    Electronic ISSN: 1753-4887
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Medicine
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  • 64
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    The Endocrine Society | Oxford University Press
    Online: 1.1987 – 30.2016
    Publisher: The Endocrine Society , Oxford University Press
    Print ISSN: 0888-8809
    Electronic ISSN: 1944-9917
    Topics: Biology , Medicine
    Acronym: MEND
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  • 65
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    Oxford University Press | HighWire Press
    Online: 1.1983 –
    Publisher: Oxford University Press , HighWire Press
    Print ISSN: 0737-4038
    Electronic ISSN: 1537-1719
    Topics: Biology
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  • 66
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    Oxford University Press | formerly Wiley-Blackwell | Elsevier / Academic Press
    Online: 116(1).1996 –
    Publisher: Oxford University Press , formerly Wiley-Blackwell , Elsevier / Academic Press
    Print ISSN: 0024-4082
    Electronic ISSN: 1096-3642
    Topics: Biology
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  • 67
    Publication Date: 2020-10-28
    Description: Fishermen are known to try to avoid fishing in stormy weather, as storms pose a physical threat to fishers, their vessels, and their gear. In this article, a dataset and methods are developed to investigate the degree to which fishers avoid storms, estimate storm aversion parameters, and explore how this response varies across vessel characteristics and across regions of the United States. The data consist of vessel-level trip-taking decisions from six federal fisheries across the United States combined with marine storm warning data from the National Weather Service. The estimates of storm aversion can be used to parameterize predictive models. Fishers’ aversion to storms decreases with increasing vessel size and increases with the severity of the storm warning. This information contributes to our understanding of the risk-to-revenue trade-off that fishers evaluate every time they consider going to sea, and of the propensity of fishers to take adaptive actions to avoid facing additional physical risk.
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
    Topics: Biology , Geosciences , Physics
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  • 68
    Publication Date: 2020-08-30
    Description: Sardine Sardinops sagax is an ecologically and economically important Clupeid found off the entire South African coast that includes both coastal upwelling and western boundary current systems. Although the management of the sardine fisheries historically assumed a single, panmictic population, the existence of three, semi-discrete subpopulations has recently been hypothesized. We conducted otolith δ18O and microstructure analyses to investigate nursery habitat temperatures and early life growth rates, respectively, of sardine collected from three biogeographic regions around South Africa’s coast to test that hypothesis. Analyses indicated that for both summer- and winter-captured adults and summer-captured juveniles, fishes from the west coast grew significantly slower in water that was several degrees cooler than those from the south and east coasts. This suggests that mixing of sardines between regions, particularly the west and other coasts, is relatively limited and supports the hypothesis of semi-discrete subpopulations. However, the west-south differences disappeared in the results for winter-captured juveniles, suggesting that differences in early life conditions between regions may change seasonally, and/or that all or most winter-captured juveniles originated from the west coast. Further elucidating the interactions between South African sardine subpopulations and the mechanisms thereof is important for sustainable harvesting of this species.
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
    Topics: Biology , Geosciences , Physics
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  • 69
    Publication Date: 2020-01-01
    Description: CerealsDB (www.cerealsdb.uk.net) is an online repository of mainly hexaploid wheat (Triticum aestivum) single nucleotide polymorphisms (SNPs) and genotyping data. The CerealsDB website has been designed to enable wheat breeders and scientists to select the appropriate markers for research breeding tasks, such as marker-assisted selection. We report a large update of genotyping information for over 6000 wheat accessions and describe new webtools for exploring and visualizing the data. We also describe a new database of quantitative trait loci that links phenotypic traits to CerealsDB SNP markers and allelic scores for each of those markers. CerealsDB is an open-access website that hosts information on wheat SNPs considered useful for both plant breeders and research scientists. The latest CerealsDB database is available at https://www.cerealsdb.uk.net/cerealgenomics/CerealsDB/indexNEW.php.
    Electronic ISSN: 1758-0463
    Topics: Biology
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  • 70
    Publication Date: 2020-10-23
    Description: Progress towards ecosystem-based fisheries management calls for useful tools to prioritize actions. To select suitable methods for local circumstances, evaluating approaches used in other jurisdictions can be a cost-effective first step. We tested Productivity Susceptibility Analysis (PSA) to assess the potential vulnerability of the marine fish community in the Skagerrak–Kattegat (Eastern North Sea) to possible interactions with all Swedish fisheries operating in the area. This analysis combines attributes for a species productivity with attributes related to the susceptibility to capture to quantify a single score for vulnerability: high, medium, or low risk. Results indicate that demersal trawl and gillnet fisheries were associated with the highest risk levels if interaction occurs, i.e. having the highest prevalence of species with potentially high vulnerability to the fisheries. Mixed results were seen when comparing the assessment results with available data. The main benefit of utilizing PSA in the area is the comprehensiveness of the assessment, including data-deficient fisheries and species. Drawbacks include potential overestimation of actual risks. Overall, together with available data, PSA in the studied area provides a comprehensive map of potential risks for further actions and may progress a science-based, precautionary management of the area.
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
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  • 71
    Publication Date: 2020-08-12
    Description: While fisheries provide food and employment for hundreds of millions of people, they also can have significant impact on biodiversity. We explore the potential of area-based fisheries management to simultaneously maintain biodiversity and high levels of sustainable food production. We used two illustrative examples of fisheries that have different gear types, areas, and species to evaluate the trade-off between biodiversity and harvest. We calculate the optimal effort by gear and area that maximizes a weighted objective function of biodiversity and harvest, ranging from 100% of the weight on harvest to 100% on biodiversity. We found for both case studies that the trade-off was highly convex, with win–win solutions allowing for high levels of both fishery harvest and conservation. This is achieved by reducing or eliminating fishing effort that negatively impacts high conservation value species while maintaining fishing effort with gears and in areas where there is low conservation impact. We suggest that, in most fisheries, such situations can be found and that effective area-based management can provide for high levels of biodiversity protection and food production.
    Print ISSN: 1054-3139
    Electronic ISSN: 1095-9289
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  • 72
    Publication Date: 2020-01-01
    Description: Repeatability of study setups and reproducibility of research results by underlying data are major requirements in science. Until now, abstract models for describing the structural logic of studies in environmental sciences are lacking and tools for data management are insufficient. Mandatory for repeatability and reproducibility is the use of sophisticated data management solutions going beyond data file sharing. Particularly, it implies maintenance of coherent data along workflows. Design data concern elements from elementary domains of operations being transformation, measurement and transaction. Operation design elements and method information are specified for each consecutive workflow segment from field to laboratory campaigns. The strict linkage of operation design element values, operation values and objects is essential. For enabling coherence of corresponding objects along consecutive workflow segments, the assignment of unique identifiers and the specification of their relations are mandatory. The abstract model presented here addresses these aspects, and the software DiversityDescriptions (DWB-DD) facilitates the management of thusly connected digital data objects and structures. DWB-DD allows for an individual specification of operation design elements and their linking to objects. Two workflow design use cases, one for DNA barcoding and another for cultivation of fungal isolates, are given. To publish those structured data, standard schema mapping and XML-provision of digital objects are essential. Schemas useful for this mapping include the Ecological Markup Language, the Schema for Meta-omics Data of Collection Objects and the Standard for Structured Descriptive Data. Data pipelines with DWB-DD include the mapping and conversion between schemas and functions for data publishing and archiving according to the Open Archival Information System standard. The setting allows for repeatability of study setups, reproducibility of study results and for supporting work groups to structure and maintain their data from the beginning of a study. The theory of ‘FAIR++’ digital objects is introduced.
    Electronic ISSN: 1758-0463
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  • 73
    Publication Date: 2020-08-08
    Description: Recent application of Fourier transform near infra-red spectroscopy (FT-NIRS) to predict age in fish otoliths has gained attention among fisheries managers as a potential alternative to costly production ageing of managed species. We assessed the age prediction capability of FT-NIRS scans in whole otoliths from red snapper, Lutjanus campechanus, collected from the US Gulf of Mexico and US Atlantic Ocean (South Atlantic). Otoliths were scanned with an FT-NIR spectrometer and resulting spectral signatures were regressed with traditionally estimated ages via partial least squares regression to produce calibration models, which were validated for predictive capability against test sets of otoliths. Calibration models successfully predicted age with R2 ranging 0.94–0.95, mean squared error ≤1.8 years, and bias 31 years were not well predicted, possibly due to light attenuation in the thickest otoliths. Our results suggest that FT-NIRS can improve efficiency in production ageing for fisheries management while maintaining data quality standards.
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  • 74
    Publication Date: 2020-10-10
    Description: This article investigates the diet of the snow crab (Chionoecetes opilio) and its feeding intensity in the Barents Sea. Data show that snow crab has a diverse diet that includes almost all types of benthic invertebrates living in the Barents Sea. There are differences between the diets of females and males and of juveniles and adults. Juveniles and females typically occupy shallow areas with communities of bivalve molluscs, while males typically live deeper on slopes and depressions where polychaetes and crustaceans are the most abundant groups. Stomach contents were analysed to determine the species composition and frequency of occurrence of various benthic taxa. Consumption of food was estimated and compared with data from the Russian seas of the Pacific region. The total annual consumption of macrozoobenthos by snow crab was calculated in accordance with its current distribution in the Barents Sea. Snow crab consumes at least 30 000 tonnes of benthos annually, which amounts to 0.1–0.2% of the total macrozoobenthic biomass in the investigated area. The population of snow crab causes the largest impact on the benthic communities in the northeastern part of the Barents Sea and near the south side of the Novaya Zemlya archipelago.
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  • 75
    Publication Date: 2020-08-24
    Description: Until the late 19th century, extensive beds of flat oyster Ostrea edulis populated the Central North Sea, which have vanished after intensive fisheries. At present, various initiatives are being carried out to investigate the potential to restore this former key species in the area. This historical ecological study contributes by delineating the former oyster bed area and through an assessment of its limits against known gradients in the North Sea. Extensive data from historical maps, texts, and ship-based surveys were used to synthesize our knowledge on the former beds. It was revealed that the area with oyster beds covered ∼6.2% of the total North Sea bottom, with a delineation that could partly be explained by hydrodynamic and temperature gradients. The position and extent of the area are notably different from the area that is used in recent feasibility studies on the restoration of North Sea oyster beds. The offshore oysters lived on muddy sand in relatively cold conditions, and there are several indications that their reproductive rate was low. The apparent disappearance of cold water adapted flat oysters will challenge restoration projects. This study provides indispensable information for the future restoration of flat oyster beds in the North Sea.
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  • 76
    Publication Date: 2015-08-08
    Description: : As sequencing becomes cheaper and more widely available, there is a greater need to quickly and effectively analyze large-scale genomic data. While the functionality of AVIA v1.0, whose implementation was based on ANNOVAR, was comparable with other annotation web servers, AVIA v2.0 represents an enhanced web-based server that extends genomic annotations to cell-specific transcripts and protein-level functional annotations. With AVIA’s improved interface, users can better visualize their data, perform comprehensive searches and categorize both coding and non-coding variants. Availability and implementation : AVIA is freely available through the web at http://avia.abcc.ncifcrf.gov . Contact : Hue.Vuong@fnlcr.nih.gov Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 77
    Publication Date: 2015-08-08
    Description: : As new methods for multivariate analysis of genome wide association studies become available, it is important to be able to combine results from different cohorts in a meta-analysis. The R package MultiMeta provides an implementation of the inverse-variance-based method for meta-analysis, generalized to an n -dimensional setting. Availability and implementation: The R package MultiMeta can be downloaded from CRAN. Contact: dragana.vuckovic@burlo.trieste.it ; vi1@sanger.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 78
    Publication Date: 2015-08-12
    Description: Some of the most dangerous pathogens such as Mycobacterium tuberculosis and Yersinia pestis evolve clonally . This means that little or no recombination occurs between strains belonging to these species. Paradoxically, although different members of these species show extreme sequence similarity of orthologous genes, some show considerable intraspecies phenotypic variation, the source of which remains elusive. To examine the possible sources of phenotypic variation within clonal pathogenic bacterial species, we carried out an extensive genomic and pan-genomic analysis of the sources of genetic variation available to a large collection of clonal and nonclonal pathogenic bacterial species. We show that while nonclonal species diversify through a combination of changes to gene sequences, gene loss and gene gain, gene loss completely dominates as a source of genetic variation within clonal species. Indeed, gene loss is so prevalent within clonal species as to lead to levels of gene content variation comparable to those found in some nonclonal species that are much more diverged in their gene sequences and that acquire a substantial number of genes horizontally. Gene loss therefore needs to be taken into account as a potential dominant source of phenotypic variation within clonal bacterial species.
    Electronic ISSN: 1759-6653
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  • 79
    Publication Date: 2015-08-12
    Description: Obligate bacterial symbionts are widespread in many invertebrates, where they are often confined to specialized host cells and are transmitted directly from mother to progeny. Increasing numbers of these bacteria are being characterized but questions remain about their population structure and evolution. Here we take a comparative genomics approach to investigate two prominent bacterial symbionts (BFo1 and BFo2) isolated from geographically separated populations of western flower thrips, Frankliniella occidentalis. Our multifaceted approach to classifying these symbionts includes concatenated multilocus sequence analysis (MLSA) phylogenies, ribosomal multilocus sequence typing (rMLST), construction of whole-genome phylogenies, and in-depth genomic comparisons. We showed that the BFo1 genome clusters more closely to species in the genus Erwinia, and is a putative close relative to Erwinia aphidicola . BFo1 is also likely to have shared a common ancestor with Erwinia pyrifoliae/Erwinia amylovora and the nonpathogenic Erwinia tasmaniensis and genetic traits similar to Erwinia billingiae . The BFo1 genome contained virulence factors found in the genus Erwinia but represented a divergent lineage. In contrast, we showed that BFo2 belongs within the Enterobacteriales but does not group closely with any currently known bacterial species. Concatenated MLSA phylogenies indicate that it may have shared a common ancestor to the Erwinia and Pantoea genera, and based on the clustering of rMLST genes, it was most closely related to Pantoea ananatis but represented a divergent lineage. We reconstructed a core genome of a putative common ancestor of Erwinia and Pantoea and compared this with the genomes of BFo bacteria. BFo2 possessed none of the virulence determinants that were omnipresent in the Erwinia and Pantoea genera. Taken together, these data are consistent with BFo2 representing a highly novel species that maybe related to known Pantoea .
    Electronic ISSN: 1759-6653
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  • 80
    Publication Date: 2015-08-16
    Description: Gene expression evolution occurs through changes in cis - or trans -regulatory elements or both. Interactions between transcription factors (TFs) and their binding sites (TFBSs) constitute one of the most important points where these two regulatory components intersect. In this study, we investigated the evolution of TFBSs in the promoter regions of different Saccharomyces strains and species. We divided the promoter of a gene into the proximal region and the distal region, which are defined, respectively, as the 200-bp region upstream of the transcription starting site and as the 200-bp region upstream of the proximal region. We found that the predicted TFBSs in the proximal promoter regions tend to be evolutionarily more conserved than those in the distal promoter regions. Additionally, Saccharomyces cerevisiae strains used in the fermentation of alcoholic drinks have experienced more TFBS losses than gains compared with strains from other environments (wild strains, laboratory strains, and clinical strains). We also showed that differences in TFBSs correlate with the cis component of gene expression evolution between species (comparing S. cerevisiae and its sister species Saccharomyces paradoxus ) and within species (comparing two closely related S. cerevisiae strains).
    Electronic ISSN: 1759-6653
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  • 81
    Publication Date: 2015-08-16
    Description: Gene duplication is a key factor contributing to phenotype diversity across and within species. Although the availability of complete genomes has led to the extensive study of genomic duplications, the dynamics and variability of gene duplications mediated by retrotransposition are not well understood. Here, we predict mRNA retrotransposition and use comparative genomics to investigate their origin and variability across primates. Analyzing seven anthropoid primate genomes, we found a similar number of mRNA retrotranspositions (~7,500 retrocopies) in Catarrhini (Old Word Monkeys, including humans), but a surprising large number of retrocopies (~10,000) in Platyrrhini (New World Monkeys), which may be a by-product of higher long interspersed nuclear element 1 activity in these genomes. By inferring retrocopy orthology, we dated most of the primate retrocopy origins, and estimated a decrease in the fixation rate in recent primate history, implying a smaller number of species-specific retrocopies. Moreover, using RNA-Seq data, we identified approximately 3,600 expressed retrocopies. As expected, most of these retrocopies are located near or within known genes, present tissue-specific and even species-specific expression patterns, and no expression correlation to their parental genes. Taken together, our results provide further evidence that mRNA retrotransposition is an active mechanism in primate evolution and suggest that retrocopies may not only introduce great genetic variability between lineages but also create a large reservoir of potentially functional new genomic loci in primate genomes.
    Electronic ISSN: 1759-6653
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  • 82
    Publication Date: 2015-08-06
    Description: Viruses rely completely on the hosts’ machinery for translation of viral transcripts. However, for most viruses infecting humans, codon usage preferences (CUPrefs) do not match those of the host. Human papillomaviruses (HPVs) are a showcase to tackle this paradox: they present a large genotypic diversity and a broad range of phenotypic presentations, from asymptomatic infections to productive lesions and cancer. By applying phylogenetic inference and dimensionality reduction methods, we demonstrate first that genes in HPVs are poorly adapted to the average human CUPrefs, the only exception being capsid genes in viruses causing productive lesions. Phylogenetic relationships between HPVs explained only a small proportion of CUPrefs variation. Instead, the most important explanatory factor for viral CUPrefs was infection phenotype, as orthologous genes in viruses with similar clinical presentation displayed similar CUPrefs. Moreover, viral genes with similar spatiotemporal expression patterns also showed similar CUPrefs. Our results suggest that CUPrefs in HPVs reflect either variations in the mutation bias or differential selection pressures depending on the clinical presentation and expression timing. We propose that poor viral CUPrefs may be central to a trade-off between strong viral gene expression and the potential for eliciting protective immune response.
    Electronic ISSN: 1759-6653
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  • 83
    Publication Date: 2015-08-07
    Description: Huntington's disease (HD) is a hereditary neurodegenerative disorder characterized by brain atrophy particularly in striatum leading to personality changes, chorea and dementia. Glycogen synthase kinase-3 (GSK-3) is a serine/threonine kinase in the crossroad of many signaling pathways that is highly pleiotropic as it phosphorylates more than hundred substrates including structural, metabolic, and signaling proteins. Increased GSK-3 activity is believed to contribute to the pathogenesis of neurodegenerative diseases like Alzheimer's disease and GSK-3 inhibitors have been postulated as therapeutic agents for neurodegeneration. Regarding HD, GSK-3 inhibitors have shown beneficial effects in cell and invertebrate animal models but no evident efficacy in mouse models. Intriguingly, those studies were performed without interrogating GSK-3 level and activity in HD brain. Here we aim to explore the level and also the enzymatic activity of GSK-3 in the striatum and other less affected brain regions of HD patients and of the R6/1 mouse model to then elucidate the possible contribution of its alteration to HD pathogenesis by genetic manipulation in mice. We report a dramatic decrease in GSK-3 levels and activity in striatum and cortex of HD patients with similar results in the mouse model. Correction of the GSK-3 deficit in HD mice, by combining with transgenic mice with conditional GSK-3 expression, resulted in amelioration of their brain atrophy and behavioral motor and learning deficits. Thus, our results demonstrate that decreased brain GSK-3 contributes to HD neurological phenotype and open new therapeutic opportunities based on increasing GSK-3 activity or attenuating the harmful consequences of its decrease.
    Print ISSN: 0964-6906
    Electronic ISSN: 1460-2083
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  • 84
    Publication Date: 2015-08-07
    Description: Spinocerebellar ataxia type 6 (SCA6) is dominantly inherited neurodegenerative disease, caused by an expansion of CAG repeat encoding a polyglutamine (PolyQ) tract in the Ca v 2.1 voltage-gated calcium channel. Its key pathological features include selective degeneration of the cerebellar Purkinje cells (PCs), a common target for PolyQ-induced toxicity in various SCAs. Mutant Ca v 2.1 confers toxicity primarily through a toxic gain-of-function mechanism; however, its molecular basis remains elusive. Here, we studied the cerebellar gene expression patterns of young Sca6 -MPI 118Q/118Q knockin (KI) mice, which expressed mutant Ca v 2.1 from an endogenous locus and recapitulated many phenotypic features of human SCA6. Transcriptional signatures in the MPI 118Q/118Q mice were distinct from those in the Sca1 154Q/2Q mice, a faithful SCA1 KI mouse model. Temporal expression profiles of the candidate genes revealed that the up-regulation of genes associated with microglial activation was initiated before PC degeneration and was augmented as the disease progressed. Histological analysis of the MPI 118Q/118Q cerebellum showed the predominance of M1-like pro-inflammatory microglia and it was concomitant with elevated expression levels of tumor necrosis factor, interleukin-6, Toll-like receptor (TLR) 2 and 7. Genetic ablation of MyD88, a major adaptor protein conveying TLR signaling, altered expression patterns of M1/M2 microglial phenotypic markers in the MPI 118Q/118Q cerebellum. More importantly, it ameliorated PC loss and partially rescued motor impairments in the early disease phase. These results suggest that early neuroinflammatory response may play an important role in the pathogenesis of SCA6 and its modulation could pave the way for slowing the disease progression during the early stage of the disease.
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  • 85
    Publication Date: 2015-08-08
    Description: Motivation: Stem cell differentiation is largely guided by master transcriptional regulators, but it also depends on the expression of other types of genes, such as cell cycle genes, signaling genes, metabolic genes, trafficking genes, etc. Traditional approaches to understanding gene expression patterns across multiple conditions, such as principal components analysis or K-means clustering, can group cell types based on gene expression, but they do so without knowledge of the differentiation hierarchy. Hierarchical clustering can organize cell types into a tree, but in general this tree is different from the differentiation hierarchy itself. Methods: Given the differentiation hierarchy and gene expression data at each node, we construct a weighted Euclidean distance metric such that the minimum spanning tree with respect to that metric is precisely the given differentiation hierarchy. We provide a set of linear constraints that are provably sufficient for the desired construction and a linear programming approach to identify sparse sets of weights, effectively identifying genes that are most relevant for discriminating different parts of the tree. Results: We apply our method to microarray gene expression data describing 38 cell types in the hematopoiesis hierarchy, constructing a weighted Euclidean metric that uses just 175 genes. However, we find that there are many alternative sets of weights that satisfy the linear constraints. Thus, in the style of random-forest training, we also construct metrics based on random subsets of the genes and compare them to the metric of 175 genes. We then report on the selected genes and their biological functions. Our approach offers a new way to identify genes that may have important roles in stem cell differentiation. Contact: tperkins@ohri.ca Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 86
    Publication Date: 2015-08-08
    Description: Motivation: Principal component analysis (PCA) is a basic tool often used in bioinformatics for visualization and dimension reduction. However, it is known that PCA may not consistently estimate the true direction of maximal variability in high-dimensional, low sample size settings, which are typical for molecular data. Assuming that the underlying signal is sparse, i.e. that only a fraction of features contribute to a principal component (PC), this estimation consistency can be retained. Most existing sparse PCA methods use L1-penalization, i.e. the lasso , to perform feature selection. But, the lasso is known to lack variable selection consistency in high dimensions and therefore a subsequent interpretation of selected features can give misleading results. Results: We present S4VDPCA, a sparse PCA method that incorporates a subsampling approach, namely stability selection. S4VDPCA can consistently select the truly relevant variables contributing to a sparse PC while also consistently estimate the direction of maximal variability. The performance of the S4VDPCA is assessed in a simulation study and compared to other PCA approaches, as well as to a hypothetical oracle PCA that ‘knows’ the truly relevant features in advance and thus finds optimal, unbiased sparse PCs. S4VDPCA is computationally efficient and performs best in simulations regarding parameter estimation consistency and feature selection consistency. Furthermore, S4VDPCA is applied to a publicly available gene expression data set of medulloblastoma brain tumors. Features contributing to the first two estimated sparse PCs represent genes significantly over-represented in pathways typically deregulated between molecular subgroups of medulloblastoma. Availability and implementation: Software is available at https://github.com/mwsill/s4vdpca . Contact: m.sill@dkfz.de Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 87
    Publication Date: 2015-08-08
    Description: Motivation: Glycans play critical roles in many biological processes, and their structural diversity is key for specific protein-glycan recognition. Comparative structural studies of biological molecules provide useful insight into their biological relationships. However, most computational tools are designed for protein structure, and despite their importance, there is no currently available tool for comparing glycan structures in a sequence order- and size-independent manner. Results: A novel method, GS-align, is developed for glycan structure alignment and similarity measurement. GS-align generates possible alignments between two glycan structures through iterative maximum clique search and fragment superposition. The optimal alignment is then determined by the maximum structural similarity score, GS-score, which is size-independent. Benchmark tests against the Protein Data Bank (PDB) N -linked glycan library and PDB homologous/non-homologous N -glycoprotein sets indicate that GS-align is a robust computational tool to align glycan structures and quantify their structural similarity. GS-align is also applied to template-based glycan structure prediction and monosaccharide substitution matrix generation to illustrate its utility. Availability and implementation: http://www.glycanstructure.org/gsalign . Contact: wonpil@ku.edu Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 88
    Publication Date: 2015-08-08
    Description: Motivation: Impedance-based technologies are advancing methods for measuring proliferation of adherent cell cultures non-invasively and in real time. The analysis of the resulting data has so far been hampered by inappropriate computational methods and the lack of systematic data to evaluate the characteristics of the assay. Results: We used a commercially available system for impedance-based growth measurement (xCELLigence) and compared the reported cell index with data from microscopy. We found that the measured signal correlates linearly with the cell number throughout the time of an experiment with sufficient accuracy in subconfluent cell cultures. The resulting growth curves for various colon cancer cells could be well described with the empirical Richards growth model, which allows for extracting quantitative parameters (such as characteristic cycle times). We found that frequently used readouts like the cell index at a specific time or the area under the growth curve cannot be used to faithfully characterize growth inhibition. We propose to calculate the average growth rate of selected time intervals to accurately estimate time-dependent IC50 values of drugs from growth curves. Contact: nils.bluethgen@charite.de Supplementary information: Supplementary data are available at Bioinformatics online.
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  • 89
    Publication Date: 2015-08-20
    Description: Spliceosomal introns are a hallmark of eukaryotic genes that are hypothesized to play important roles in genome evolution but have poorly understood origins. Although most introns lack sequence homology to each other, new families of spliceosomal introns that are repeated hundreds of times in individual genomes have recently been discovered in a few organisms. The prevalence and conservation of these introner elements (IEs) or introner-like elements in other taxa, as well as their evolutionary relationships to regular spliceosomal introns, are still unknown. Here, we systematically investigate introns in the widespread marine green alga Micromonas and report new families of IEs, numerous intron presence–absence polymorphisms, and potential intron insertion hot-spots. The new families enabled identification of conserved IE secondary structure features and establishment of a novel general model for repetitive intron proliferation across genomes. Despite shared secondary structure, the IE families from each Micromonas lineage bear no obvious sequence similarity to those in the other lineages, suggesting that their appearance is intimately linked with the process of speciation. Two of the new IE families come from an Arctic culture ( Micromonas Clade E2) isolated from a polar region where abundance of this alga is increasing due to climate induced changes. The same two families were detected in metagenomic data from Antarctica—a system where Micromonas has never before been reported. Strikingly high identity between the Arctic isolate and Antarctic coding sequences that flank the IEs suggests connectivity between populations in the two polar systems that we postulate occurs through deep-sea currents. Recovery of Clade E2 sequences in North Atlantic Deep Waters beneath the Gulf Stream supports this hypothesis. Our research illuminates the dynamic relationships between an unusual class of repetitive introns, genome evolution, speciation, and global distribution of this sentinel marine alga.
    Print ISSN: 0737-4038
    Electronic ISSN: 1537-1719
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  • 90
    Publication Date: 2015-08-20
    Description: Cellular Ca 2+ homeostasis is tightly regulated and is pivotal to life. Inositol 1,4,5-trisphosphate receptors (IP 3 Rs) and ryanodine receptors (RyRs) are the major ion channels that regulate Ca 2+ release from intracellular stores. Although these channels have been extensively investigated in multicellular organisms, an appreciation of their evolution and the biology of orthologs in unicellular organisms is largely lacking. Extensive phylogenetic analyses reveal that the IP 3 R gene superfamily is ancient and diverged into two subfamilies, IP 3 R-A and IP 3 R-B/RyR, at the dawn of Opisthokonta. IP 3 R-B/RyR further diversified into IP 3 R-B and RyR at the stem of Filozoa. Subsequent evolution and speciation of Holozoa is associated with duplication of IP 3 R-A and RyR genes, and loss of IP 3 R-B in the vertebrate lineages. To gain insight into the properties of IP 3 R important for the challenges of multicellularity, the IP 3 R-A and IP 3 R-B family orthologs were cloned from Capsaspora owczarzaki, a close unicellular relative to Metazoa (designated as CO.IP 3 R-A and CO.IP 3 R-B). Both proteins were targeted to the endoplasmic reticulum. However, CO.IP 3 R-A, but strikingly not CO.IP 3 R-B, bound IP 3 , exhibited robust Ca 2+ release activity and associated with mammalian IP 3 Rs. These data indicate strongly that CO.IP 3 R-A as an exemplar of ancestral IP 3 R-A orthologs forms bona fide IP 3 -gated channels. Notably, however, CO.IP 3 R-A appears not to be regulated by Ca 2+ , ATP or Protein kinase A-phosphorylation. Collectively, our findings explore the origin, conservation, and diversification of IP 3 R gene families and provide insight into the functionality of ancestral IP 3 Rs and the added specialization of these proteins in Metazoa.
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  • 91
    Publication Date: 2015-08-20
    Description: Marriage rules, the community prescriptions that dictate who an individual can or cannot marry, are extremely diverse and universally present in traditional societies. A major focus of research in the early decades of modern anthropology, marriage rules impose social and economic forces that help structure societies and forge connections between them. However, in those early anthropological studies, the biological benefits or disadvantages of marriage rules could not be determined. We revisit this question by applying a novel simulation framework and genome-wide data to explore the effects of Asymmetric Prescriptive Alliance, an elaborate set of marriage rules that has been a focus of research for many anthropologists. Simulations show that strict adherence to these marriage rules reduces genetic diversity on the autosomes, X chromosome and mitochondrial DNA, but relaxed compliance produces genetic diversity similar to random mating. Genome-wide data from the Indonesian community of Rindi, one of the early study populations for Asymmetric Prescriptive Alliance, are more consistent with relaxed compliance than strict adherence. We therefore suggest that, in practice, marriage rules are treated with sufficient flexibility to allow social connectivity without significant degradation of biological diversity.
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  • 92
    Publication Date: 2015-08-20
    Description: The environment has profound effects on the expression of many traits and reaction norms describe the expression dynamics of a trait across a broad range of environmental conditions. Here, we analyze gene expression in Drosophila melanogaster across four different developmental temperatures (13–29 °C). Gene expression is highly plastic with 83.3% of the genes being differentially expressed. We distinguished three components of plasticity: 1) Dynamics of gene expression intensity (sum of change), 2) direction of change, and 3) curvature of the reaction norm (linear vs. quadratic). Studying their regulatory architecture we found that all three plasticity components were most strongly affected by the number of different transcription factors (TFs) binding to the target gene. More TFs were found in genes with less expression changes across temperatures. Although the effect of microRNAs was weaker, we consistently noted a trend in the opposite direction. The most plastic genes were regulated by fewer TFs and more microRNAs than less plastic genes. Different patterns of plasticity were also reflected by their functional characterization based on gene ontology. Our results suggest that reaction norms provide an important key to understand the functional requirements of natural populations exposed to variable environmental conditions.
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  • 93
    Publication Date: 2015-08-20
    Description: Recent advances in paleogenomic technologies have enabled an increasingly detailed understanding of the evolutionary relationships of now-extinct mammalian taxa. However, a number of enigmatic Quaternary species have never been characterized with molecular data, often because available fossils are rare or are found in environments that are not optimal for DNA preservation. Here, we analyze paleogenomic data extracted from bones attributed to the late Pleistocene western camel, Camelops cf. hesternus, a species that was distributed across central and western North America until its extinction approximately 13,000 years ago. Despite a modal sequence length of only around 35 base pairs, we reconstructed high-coverage complete mitochondrial genomes and low-coverage partial nuclear genomes for each specimen. We find that Camelops is sister to African and Asian bactrian and dromedary camels, to the exclusion of South American camelids (llamas, guanacos, alpacas, and vicuñas). These results contradict previous morphology-based phylogenetic models for Camelops , which suggest instead a closer relationship between Camelops and the South American camelids. The molecular data imply a Late Miocene divergence of the Camelops clade from lineages that separately gave rise to the extant camels of Eurasia. Our results demonstrate the increasing capacity of modern paleogenomic methods to resolve evolutionary relationships among distantly related lineages.
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  • 94
    Publication Date: 2015-08-20
    Description: Recent developments in the analysis of amino acid covariation are leading to breakthroughs in protein structure prediction, protein design, and prediction of the interactome. It is assumed that observed patterns of covariation are caused by molecular coevolution, where substitutions at one site affect the evolutionary forces acting at neighboring sites. Our theoretical and empirical results cast doubt on this assumption. We demonstrate that the strongest coevolutionary signal is a decrease in evolutionary rate and that unfeasibly long times are required to produce coordinated substitutions. We find that covarying substitutions are mostly found on different branches of the phylogenetic tree, indicating that they are independent events that may or may not be attributable to coevolution. These observations undermine the hypothesis that molecular coevolution is the primary cause of the covariation signal. In contrast, we find that the pairs of residues with the strongest covariation signal tend to have low evolutionary rates, and that it is this low rate that gives rise to the covariation signal. Slowly evolving residue pairs are disproportionately located in the protein’s core, which explains covariation methods’ ability to detect pairs of residues that are close in three dimensions. These observations lead us to propose the "coevolution paradox": The strength of coevolution required to cause coordinated changes means the evolutionary rate is so low that such changes are highly unlikely to occur. As modern covariation methods may lead to breakthroughs in structural genomics, it is critical to recognize their biases and limitations.
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  • 95
    Publication Date: 2015-08-20
    Description: We present a modified GPU (graphics processing unit) version of MrBayes, called ta(MC) 3 (GPU MrBayes V3.1), for Bayesian phylogenetic inference on protein data sets. Our main contributions are 1) utilizing 64-bit variables, thereby enabling ta(MC) 3 to process larger data sets than MrBayes; and 2) to use Kahan summation to improve accuracy, convergence rates, and consequently runtime. Versus the current fastest software, we achieve a speedup of up to around 2.5 (and up to around 90 vs. serial MrBayes), and more on multi-GPU hardware. GPU MrBayes V3.1 is available from http://sourceforge.net/projects/mrbayes-gpu/ .
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  • 96
    Publication Date: 2015-08-20
    Description: Understanding the genetic and molecular bases of the ability to distinguish self from nonself (allorecognition) and mechanisms underlying evolution of allorecognition systems is an important endeavor for understanding cases where it becomes dysfunctional, such as in autoimmune disorders. In filamentous fungi, allorecognition can result in vegetative or heterokaryon incompatibility, which is a type of programmed cell death that occurs following fusion of genetically different cells. Allorecognition is genetically controlled by het loci, with coexpression of any combination of incompatible alleles triggering vegetative incompatibility. Herein, we identified, characterized, and inferred the evolutionary history of candidate het loci in the filamentous fungus Neurospora crassa . As characterized het loci encode proteins carrying an HET domain, we annotated HET domain genes in 25 isolates from a natural population along with the N. crassa reference genome using resequencing data. Because allorecognition systems can be affected by frequency-dependent selection favoring rare alleles (i.e., balancing selection), we mined resequencing data for HET domain loci whose alleles displayed elevated levels of variability, excess of intermediate frequency alleles, and deep gene genealogies. From these analyses, 34 HET domain loci were identified as likely to be under balancing selection. Using transformation, incompatibility assays and genetic analyses, we determined that one of these candidates functioned as a het locus ( het-e ). The het-e locus has three divergent allelic groups that showed signatures of positive selection, intra- and intergroup recombination, and trans-species polymorphism. Our findings represent a compelling case of balancing selection functioning on multiple alleles across multiple loci potentially involved in allorecognition.
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  • 97
    Publication Date: 2015-08-20
    Description: Scoring the impact of noncoding variation on the function of cis -regulatory regions, on their chromatin state, and on the qualitative and quantitative expression levels of target genes is a fundamental problem in evolutionary genomics. A particular challenge is how to model the divergence of quantitative traits and to identify relationships between the changes across the different levels of the genome, the chromatin activity landscape, and the transcriptome. Here, we examine the use of the Ornstein–Uhlenbeck (OU) model to infer selection at the level of predicted cis -regulatory modules (CRMs), and link these with changes in transcription factor binding and chromatin activity. Using publicly available cross-species ChIP-Seq and STARR-Seq data we show how OU can be applied genome-wide to identify candidate transcription factors for which binding site and CRM turnover is correlated with changes in regulatory activity. Next, we profile open chromatin in the developing eye across three Drosophila species. We identify the recognition motifs of the chromatin remodelers, Trithorax-like and Grainyhead as mostly correlating with species-specific changes in open chromatin. In conclusion, we show in this study that CRM scores can be used as quantitative traits and that motif discovery approaches can be extended towards more complex models of divergence.
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  • 98
    Publication Date: 2015-08-20
    Description: How populations that inhabit the same geographical area become genetically differentiated is not clear. To investigate this, we characterized phenotypic and genetic differences between two populations of Saccharomyces cerevisiae that in some cases inhabit the same environment but show relatively little gene flow. We profiled stress sensitivity in a group of vineyard isolates and a group of oak-soil strains and found several niche-related phenotypes that distinguish the populations. We performed bulk-segregant mapping on two of the distinguishing traits: The vineyard-specific ability to grow in grape juice and oak-specific tolerance to the cell wall damaging drug Congo red. To implicate causal genes, we also performed a chemical genomic screen in the lab-strain deletion collection and identified many important genes that fell under quantitative trait loci peaks. One gene important for growth in grape juice and identified by both the mapping and the screen was SSU1 , a sulfite-nitrite pump implicated in wine fermentations. The beneficial allele is generated by a known translocation that we reasoned may also serve as a genetic barrier. We found that the translocation is prevalent in vineyard strains, but absent in oak strains, and presents a postzygotic barrier to spore viability. Furthermore, the translocation was associated with a fitness cost to the rapid growth rate seen in oak-soil strains. Our results reveal the translocation as a dual-function locus that enforces ecological differentiation while producing a genetic barrier to gene flow in these sympatric populations.
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  • 99
    Publication Date: 2015-08-20
    Description: Species tree reconstruction has been a subject of substantial research due to its central role across biology and medicine. A species tree is often reconstructed using a set of gene trees or by directly using sequence data. In either of these cases, one of the main confounding phenomena is the discordance between a species tree and a gene tree due to evolutionary events such as duplications and losses. Probabilistic methods can resolve the discordance by coestimating gene trees and the species tree but this approach poses a scalability problem for larger data sets. We present MixTreEM-DLRS: A two-phase approach for reconstructing a species tree in the presence of gene duplications and losses. In the first phase, MixTreEM, a novel structural expectation maximization algorithm based on a mixture model is used to reconstruct a set of candidate species trees, given sequence data for monocopy gene families from the genomes under study. In the second phase, PrIME-DLRS, a method based on the DLRS model (Åkerborg O, Sennblad B, Arvestad L, Lagergren J. 2009. Simultaneous Bayesian gene tree reconstruction and reconciliation analysis. Proc Natl Acad Sci U S A. 106(14):5714–5719), is used for selecting the best species tree. PrIME-DLRS can handle multicopy gene families since DLRS, apart from modeling sequence evolution, models gene duplication and loss using a gene evolution model (Arvestad L, Lagergren J, Sennblad B. 2009. The gene evolution model and computing its associated probabilities. J ACM. 56(2):1–44). We evaluate MixTreEM-DLRS using synthetic and biological data, and compare its performance with a recent genome-scale species tree reconstruction method PHYLDOG ( Boussau B, Szöllősi GJ, Duret L, Gouy M, Tannier E, Daubin V. 2013 . Genome-scale coestimation of species and gene trees. Genome Res. 23(2):323–330) as well as with a fast parsimony-based algorithm Duptree (Wehe A, Bansal MS, Burleigh JG, Eulenstein O. 2008. Duptree: a program for large-scale phylogenetic analyses using gene tree parsimony. Bioinformatics 24(13):1540–1541). Our method is competitive with PHYLDOG in terms of accuracy and runs significantly faster and our method outperforms Duptree in accuracy. The analysis constituted by MixTreEM without DLRS may also be used for selecting the target species tree, yielding a fast and yet accurate algorithm for larger data sets. MixTreEM is freely available at http://prime.scilifelab.se/mixtreem/ .
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  • 100
    Publication Date: 2015-08-20
    Description: Contrasting with birds and mammals, poikilothermic vertebrates often have homomorphic sex chromosomes, possibly resulting from high rates of sex-chromosome turnovers and/or occasional X–Y recombination. Strong support for the latter mechanism was provided by four species of European tree frogs, which inherited from a common ancestor (~5 Ma) the same pair of homomorphic sex chromosomes (linkage group 1, LG1), harboring the candidate sex-determining gene Dmrt1. Here, we test sex linkage of LG1 across six additional species of the Eurasian Hyla radiation with divergence times ranging from 6 to 40 Ma. LG1 turns out to be sex linked in six of nine resolved cases. Mapping the patterns of sex linkage to the Hyla phylogeny reveals several transitions in sex-determination systems within the last 10 My, including one switch in heterogamety. Phylogenetic trees of DNA sequences along LG1 are consistent with occasional X–Y recombination in all species where LG1 is sex linked. These patterns argue against one of the main potential causes for turnovers, namely the accumulation of deleterious mutations on nonrecombining chromosomes. Sibship analyses show that LG1 recombination is strongly reduced in males from most species investigated, including some in which it is autosomal. Intrinsically low male recombination might facilitate the evolution of male heterogamety, and the presence of important genes from the sex-determination cascade might predispose LG1 to become a sex chromosome.
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