Works matching IS 13674803 AND DT 2017 AND VI 33 AND IP 22
Results: 32
An introduction to deep learning on biological sequence data: examples and solutions.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3685, doi. 10.1093/bioinformatics/btx531
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MFIB: a repository of protein complexes with mutual folding induced by binding.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3682, doi. 10.1093/bioinformatics/btx486
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Multimodal mechanistic signatures for neurodegenerative diseases (NeuroMMSig): a web server for mechanism enrichment.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3679, doi. 10.1093/bioinformatics/btx399
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myVCF: a desktop application for highthroughput mutations data management.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3676, doi. 10.1093/bioinformatics/btx475
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ComplexViewer: visualization of curated macromolecular complexes.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3673, doi. 10.1093/bioinformatics/btx497
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CausalR: extracting mechanistic sense from genome scale data.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3670, doi. 10.1093/bioinformatics/btx425
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SPATKIN: a simulator for rule-based modeling of biomolecular site dynamics on surfaces.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3667, doi. 10.1093/bioinformatics/btx456
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DynaPho: a web platform for inferring the dynamics of time-series phosphoproteomics.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3664, doi. 10.1093/bioinformatics/btx443
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DelPhiForce web server: electrostatic forces and energy calculations and visualization.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3661, doi. 10.1093/bioinformatics/btx495
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FAF-Drugs4: free ADME-tox filtering computations for chemical biology and early stages drug discovery.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3658, doi. 10.1093/bioinformatics/btx491
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3DBIONOTES v2.0: a web server for the automatic annotation of macromolecular structures.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3655, doi. 10.1093/bioinformatics/btx483
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LRCstats, a tool for evaluating long reads correction methods.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3652, doi. 10.1093/bioinformatics/btx489
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CrocoBLAST: Running BLAST efficiently in the age of next-generation sequencing.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3648, doi. 10.1093/bioinformatics/btx465
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ggseqlogo: a versatile R package for drawing sequence logos.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3645, doi. 10.1093/bioinformatics/btx469
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pgRNAFinder: a web-based tool to design distance independent paired-gRNA.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3642, doi. 10.1093/bioinformatics/btx472
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Phylotyper: in silico predictor of gene subtypes.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3638, doi. 10.1093/bioinformatics/btx459
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gVolante for standardizing completeness assessment of genome and transcriptome assemblies.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3635, doi. 10.1093/bioinformatics/btx445
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BiobankUniverse: automatic matchmaking between datasets for biobank data discovery and integration.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3627, doi. 10.1093/bioinformatics/btx478
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Improved prediction of breast cancer outcome by identifying heterogeneous biomarkers.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3619, doi. 10.1093/bioinformatics/btx487
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The value of prior knowledge in machine learning of complex network systems.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3610, doi. 10.1093/bioinformatics/btx438
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Standardizing biomass reactions and ensuring complete mass balance in genome-scale metabolic models.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3603, doi. 10.1093/bioinformatics/btx453
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TSGSIS: a high-dimensional grouped variable selection approach for detection of whole-genome SNP-SNP interactions.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3595, doi. 10.1093/bioinformatics/btx409
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A robust DF-REML framework for variance components estimation in genetic studies.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3584, doi. 10.1093/bioinformatics/btx457
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Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3575, doi. 10.1093/bioinformatics/btx480
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Prediction and modeling of pre-analytical sampling errors as a strategy to improve plasma NMR metabolomics data.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3567, doi. 10.1093/bioinformatics/btx442
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Towards clinically more relevant dissection of patient heterogeneity via survival-based Bayesian clustering.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3558, doi. 10.1093/bioinformatics/btx464
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Analysis and prediction of protein folding energy changes upon mutation by element specific persistent homology.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3549, doi. 10.1093/bioinformatics/btx460
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SPRINT: an SNP-free toolkit for identifying RNA editing sites.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3538, doi. 10.1093/bioinformatics/btx473
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Motif independent identification of potential RNA G-quadruplexes by G4RNA screener.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3532, doi. 10.1093/bioinformatics/btx498
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pLoc-mAnimal: predict subcellular localization of animal proteins with both single and multiple sites.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3524, doi. 10.1093/bioinformatics/btx476
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iDNA4mC: identifying DNA N<sup>4</sup>-methylcytosine sites based on nucleotide chemical properties.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3518, doi. 10.1093/bioinformatics/btx479
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Reference genome assessment from a population scale perspective: an accurate profile of variability and noise.
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- Bioinformatics, 2017, v. 33, n. 22, p. 3511, doi. 10.1093/bioinformatics/btx482
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