Works matching IS 13674803 AND DT 2013 AND VI 29 AND IP 17
Results: 26
Charge asymmetry in the proteins of the outer membrane.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2122, doi. 10.1093/bioinformatics/btt355
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Linc2GO: a human LincRNA function annotation resource based on ceRNA hypothesis.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2221, doi. 10.1093/bioinformatics/btt361
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Joint analysis of expression profiles from multiple cancers improves the identification of microRNA–gene interactions.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2137, doi. 10.1093/bioinformatics/btt341
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The human genome contracts again.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2199, doi. 10.1093/bioinformatics/btt362
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CellMix: a comprehensive toolbox for gene expression deconvolution.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2211, doi. 10.1093/bioinformatics/btt351
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Optimizing multiple sequence alignments using a genetic algorithm based on three objectives: structural information, non-gaps percentage and totally conserved columns.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2112
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Mechanistic insights into mutually exclusive splicing in dynamin 1.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2084, doi. 10.1093/bioinformatics/btt368
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Differential gene expression analysis using coexpression and RNA-Seq data.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2153, doi. 10.1093/bioinformatics/btt363
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Co-regulation in embryonic stem cells via context-dependent binding of transcription factors.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2162, doi. 10.1093/bioinformatics/btt365
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Flux balance impact degree: a new definition of impact degree to properly treat reversible reactions in metabolic networks.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2178, doi. 10.1093/bioinformatics/btt364
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A genomic random interval model for statistical analysis of genomic lesion data.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2088, doi. 10.1093/bioinformatics/btt372
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A Sensitive and Accurate protein domain cLassification Tool (SALT) for short reads.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2103, doi. 10.1093/bioinformatics/btt357
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Pipit: visualizing functional impacts of structural variations.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2206, doi. 10.1093/bioinformatics/btt367
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Data-based filtering for replicated high-throughput transcriptome sequencing experiments.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2146, doi. 10.1093/bioinformatics/btt350
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GRN2SBML: automated encoding and annotation of inferred gene regulatory networks complying with SBML.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2216, doi. 10.1093/bioinformatics/btt370
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Metingear: a development environment for annotating genome-scale metabolic models.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2213, doi. 10.1093/bioinformatics/btt342
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Harnessing virtual machines to simplify next-generation DNA sequencing analysis.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2075, doi. 10.1093/bioinformatics/btt352
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Quikr: a method for rapid reconstruction of bacterial communities via compressive sensing.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2096, doi. 10.1093/bioinformatics/btt336
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Cake: a bioinformatics pipeline for the integrated analysis of somatic variants in cancer genomes.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2208, doi. 10.1093/bioinformatics/btt371
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ChroMoS: an integrated web tool for SNP classification, prioritization and functional interpretation.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2197, doi. 10.1093/bioinformatics/btt356
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GPViz: dynamic visualization of genomic regions and variants affecting protein domains.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2195, doi. 10.1093/bioinformatics/btt354
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SbacHTS: Spatial background noise correction for High-Throughput RNAi Screening.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2218, doi. 10.1093/bioinformatics/btt358
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Topologically inferring risk-active pathways toward precise cancer classification by directed random walk.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2169, doi. 10.1093/bioinformatics/btt373
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cisExpress: motif detection in DNA sequences.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2203, doi. 10.1093/bioinformatics/btt366
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Towards building a disease-phenotype knowledge base: extracting disease-manifestation relationship from literature.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2186
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A new framework for computational protein design through cost function network optimization.
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- Bioinformatics, 2013, v. 29, n. 17, p. 2129, doi. 10.1093/bioinformatics/btt374
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