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  • Articles  (109)
  • Latest Papers from Table of Contents or Articles in Press  (109)
  • Articles: DFG German National Licenses
  • Oxford University Press  (109)
  • American Geophysical Union
  • Arctic Institute of North America
  • International Union of Crystallography (IUCr)
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  • Articles  (109)
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  • Latest Papers from Table of Contents or Articles in Press  (109)
  • Articles: DFG German National Licenses
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  • 1
    Publication Date: 2016-07-16
    Description: Molecular interrogation of a biological sample through DNA sequencing, RNA and microRNA profiling, proteomics and other assays, has the potential to provide a systems level approach to predicting treatment response and disease progression, and to developing precision therapies. Large publicly funded projects have generated extensive and freely available multi-assay data resources; however, bioinformatic and statistical methods for the analysis of such experiments are still nascent. We review multi-assay genomic data resources in the areas of clinical oncology, pharmacogenomics and other perturbation experiments, population genomics and regulatory genomics and other areas, and tools for data acquisition. Finally, we review bioinformatic tools that are explicitly geared toward integrative genomic data visualization and analysis. This review provides starting points for accessing publicly available data and tools to support development of needed integrative methods.
    Print ISSN: 1467-5463
    Electronic ISSN: 1477-4054
    Topics: Biology , Computer Science
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  • 2
    Publication Date: 2013-09-26
    Description: We consider the expressive power of the first-order structure 〈, C 〉 where is either of two of different domains of extended regions in Euclidean space, and C(x,y) is the topological relation ‘Region x is in contact with region y .’ We prove two main theorems: Let $$\mathcal{P}$$ [Q] be the domain of bounded, non-empty, rational polyhedra in two- or three-dimensional Euclidean space. A relation over $$\mathcal{P}$$ [Q] is definable in the structure 〈 $$\mathcal{P}$$ [Q], C 〉 if and only if is arithmetic and invariant under rational PL-homeomorphisms of the space to itself. We also extend this result to a number of other domains, including the domain of all polyhedra and the domain of semi-algebraic regions. Let $$\mathcal{R}$$ be the space of bounded, non-empty, closed regular regions in n -dimensional Euclidean space. Any analytical relation over lower dimensional (i.e. empty interior) compact point sets that is invariant under homeomorphism is implicitly definable in the structure 〈 $$\mathcal{R}$$ , C 〉.
    Print ISSN: 0955-792X
    Electronic ISSN: 1465-363X
    Topics: Computer Science , Mathematics
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  • 3
    Publication Date: 2015-05-12
    Description: Motivation: Proteins underlay the functioning of a cell and the wiring of proteins in protein–protein interaction network (PIN) relates to their biological functions. Proteins with similar wiring in the PIN ( topology around them) have been shown to have similar functions. This property has been successfully exploited for predicting protein functions. Topological similarity is also used to guide network alignment algorithms that find similarly wired proteins between PINs of different species; these similarities are used to transfer annotation across PINs, e.g. from model organisms to human. To refine these functional predictions and annotation transfers, we need to gain insight into the variability of the topology-function relationships. For example, a function may be significantly associated with specific topologies, while another function may be weakly associated with several different topologies. Also, the topology-function relationships may differ between different species. Results: To improve our understanding of topology-function relationships and of their conservation among species, we develop a statistical framework that is built upon canonical correlation analysis. Using the graphlet degrees to represent the wiring around proteins in PINs and gene ontology (GO) annotations to describe their functions, our framework: (i) characterizes statistically significant topology-function relationships in a given species, and (ii) uncovers the functions that have conserved topology in PINs of different species, which we term topologically orthologous functions. We apply our framework to PINs of yeast and human, identifying seven biological process and two cellular component GO terms to be topologically orthologous for the two organisms. Availability and implementation: http://bio-nets.doc.ic.ac.uk/goCCA.zip Contact: natasha@imperial.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.
    Print ISSN: 1367-4803
    Electronic ISSN: 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 4
    Publication Date: 2015-04-12
    Description: Motivation: Expression quantitative trait loci (eQTL) studies have discovered thousands of genetic variants that regulate gene expression, enabling a better understanding of the functional role of non-coding sequences. However, eQTL studies are costly, requiring large sample sizes and genome-wide genotyping of each sample. In contrast, analysis of allele-specific expression (ASE) is becoming a popular approach to detect the effect of genetic variation on gene expression, even within a single individual. This is typically achieved by counting the number of RNA-seq reads matching each allele at heterozygous sites and testing the null hypothesis of a 1:1 allelic ratio. In principle, when genotype information is not readily available, it could be inferred from the RNA-seq reads directly. However, there are currently no existing methods that jointly infer genotypes and conduct ASE inference, while considering uncertainty in the genotype calls. Results: We present QuASAR, quantitative allele-specific analysis of reads, a novel statistical learning method for jointly detecting heterozygous genotypes and inferring ASE. The proposed ASE inference step takes into consideration the uncertainty in the genotype calls, while including parameters that model base-call errors in sequencing and allelic over-dispersion. We validated our method with experimental data for which high-quality genotypes are available. Results for an additional dataset with multiple replicates at different sequencing depths demonstrate that QuASAR is a powerful tool for ASE analysis when genotypes are not available. Availability and implementation: http://github.com/piquelab/QuASAR . Contact: fluca@wayne.edu or rpique@wayne.edu Supplementary information: Supplementary Material is available at Bioinformatics online.
    Print ISSN: 1367-4803
    Electronic ISSN: 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 5
    Publication Date: 2015-05-26
    Description: The evolution equations for a small spherical low-Reynolds-number swimmer actuated by means of an imposed treadmilling action on its surface are derived by means of an asymptotic analysis. The analysis rests on the assumption that the swimmer radius is small compared with its distance from the wall. It generalizes, to the more realistic 3D case, recent work on 2D treadmilling swimmers near a no-slip wall. The study is motivated by a recent work on the dynamics of Volvox algae near solid surfaces.
    Print ISSN: 0272-4960
    Electronic ISSN: 1464-3634
    Topics: Mathematics
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  • 6
    Publication Date: 2012-12-21
    Description: Motivation: Accurate alignment of high-throughput RNA-seq data is a challenging and yet unsolved problem because of the non-contiguous transcript structure, relatively short read lengths and constantly increasing throughput of the sequencing technologies. Currently available RNA-seq aligners suffer from high mapping error rates, low mapping speed, read length limitation and mapping biases. Results: To align our large (〉80 billon reads) ENCODE Transcriptome RNA-seq dataset, we developed the Spliced Transcripts Alignment to a Reference (STAR) software based on a previously undescribed RNA-seq alignment algorithm that uses sequential maximum mappable seed search in uncompressed suffix arrays followed by seed clustering and stitching procedure. STAR outperforms other aligners by a factor of 〉50 in mapping speed, aligning to the human genome 550 million 2 x 76 bp paired-end reads per hour on a modest 12-core server, while at the same time improving alignment sensitivity and precision. In addition to unbiased de novo detection of canonical junctions, STAR can discover non-canonical splices and chimeric (fusion) transcripts, and is also capable of mapping full-length RNA sequences. Using Roche 454 sequencing of reverse transcription polymerase chain reaction amplicons, we experimentally validated 1960 novel intergenic splice junctions with an 80–90% success rate, corroborating the high precision of the STAR mapping strategy. Availability and implementation: STAR is implemented as a standalone C++ code. STAR is free open source software distributed under GPLv3 license and can be downloaded from http://code.google.com/p/rna-star/ . Contact: dobin@cshl.edu .
    Print ISSN: 1367-4803
    Electronic ISSN: 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 7
    Publication Date: 2013-01-18
    Description: A boundary-element method for Stokes flow is implemented to determine the drag force exerted on spherical, spheroidal, and cylindrical particles in periodic axisymmetric flow through a cylindrical tube. The pressure drop due to the motion of the particles in an otherwise quiescent fluid or due to the presence of the particles in Poiseuille flow is calculated in terms of the particle surface traction using an integral formulation. The computed drag and pressure coefficients are used to evaluate the hematocrit ratio of freely suspended particles, defined as the ratio of the mean velocity of the one-dimensional suspension to the particle velocity, and the apparent suspension viscosity. Numerical results are presented for an extended range of particle sizes and separations, and critical comparisons are made with available numerical and asymptotic solutions. In the case of freely suspended spherical particles, accurate correlations are presented for the hematocrit ratio and apparent intrinsic viscosity. The numerical results for cylindrical particles are consistent with analytical expressions based on the assumption of locally unidirectional flow. The results are discussed with reference to the numerical simulation of the flow of a suspension through a small capillary tube where the particle separation varies slowly along the tube axis.
    Print ISSN: 0272-4960
    Electronic ISSN: 1464-3634
    Topics: Mathematics
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  • 8
    Publication Date: 2016-01-23
    Description: The action dimension of a discrete group $\Gamma $ is the smallest dimension of a contractible manifold that admits a proper action of $\Gamma $ . Associated to any flag complex $L$ there is a right-angled Artin group, $A_L$ . We compute the action dimension of $A_L$ for many $L$ . Our calculations come close to confirming the conjecture that if an $\ell ^2$ -Betti number of $A_L$ in degree $l$ is nonzero, then the action dimension of $A_L$ is $\geqslant 2l$ .
    Print ISSN: 0024-6093
    Electronic ISSN: 1469-2120
    Topics: Mathematics
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  • 9
    Publication Date: 2012-04-28
    Description: : High-throughput genome-wide studies of alternatively spliced mRNA transcripts have become increasingly important in clinical research. Consequently, easy-to-use software tools are required to process data from these studies, for example, using exon and junction arrays. Here, we introduce JETTA, an integrated software package for the calculation of gene expression indices as well as the identification and visualization of alternative splicing events. We demonstrate the software using data of human liver and muscle samples hybridized on an exon–junction array. Availability: JETTA and its demonstrations are freely available at http://igenomed.stanford.edu/~junhee/JETTA/index.html Contacts: wxiao1@partners.org
    Print ISSN: 1367-4803
    Electronic ISSN: 1460-2059
    Topics: Biology , Computer Science , Medicine
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  • 10
    Publication Date: 2011-11-24
    Description: Let G be a profinite group, { X α } α be a cofiltered diagram of discrete G -spectra, and Z be a spectrum with trivial G -action. We show how to define the homotopy fixed point spectrum F ( Z , holim α X α ) hG and that when G has finite virtual cohomological dimension (vcd), it is equivalent to F ( Z , holim α ( X α ) hG ). With these tools, we show that the K ( n )-local Spanier–Whitehead dual is always a homotopy fixed point spectrum, a well-known Adams-type spectral sequence is actually a descent spectral sequence, and, for a sufficiently nice k -local profinite G -Galois extension E , with K G and closed, the equivalence (due to Behrens and the author), where denotes k -local homotopy fixed points, can be upgraded to an equivalence that just uses ordinary ( non-local ) homotopy fixed points, when G / K has finite vcd.
    Print ISSN: 0024-6093
    Electronic ISSN: 1469-2120
    Topics: Mathematics
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