GenPipes: an open-source framework for distributed and scalable genomic analyses
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Mathieu Bourgey | Rola Dali | Robert Eveleigh | Kuang Chung Chen | Louis Letourneau | Joel Fillon | Marc Michaud | Maxime Caron | Johanna Sandoval | Francois Lefebvre | Gary Leveque | Eloi Mercier | David Bujold | Pascale Marquis | Patrick Tran Van | David Anderson de Lima Morais | Julien Tremblay | Xiaojian Shao | Edouard Henrion | Emmanuel Gonzalez | Pierre-Olivier Quirion | Bryan Caron | Guillaume Bourque | P. Quirion | G. Bourque | R. Dali | F. Lefebvre | M. Caron | R. Eveleigh | Xiaojian Shao | David Bujold | Eloi Mercier | G. Leveque | J. Tremblay | M. Bourgey | Louis Letourneau | P. Van | P. Marquis | Kuang Chung Chen | J. Fillon | Bryan Caron | Marc Michaud | Johanna Sandoval | David Anderson de Lima Morais | Emmanuel Gonzalez | Édouard Henrion | Joël Fillon
[1] Sohrab P. Shah,et al. Kronos: a workflow assembler for genome analytics and informatics , 2016, bioRxiv.
[2] Ryan M. Layer,et al. LUMPY: a probabilistic framework for structural variant discovery , 2012, Genome Biology.
[3] C. Glass,et al. Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. , 2010, Molecular cell.
[4] Mark Yandell,et al. Wham: Identifying Structural Variants of Biological Consequence , 2015, PLoS Comput. Biol..
[5] Ben Nichols,et al. Distributed under Creative Commons Cc-by 4.0 Vsearch: a Versatile Open Source Tool for Metagenomics , 2022 .
[6] Bernard J. Pope,et al. Bpipe: a tool for running and managing bioinformatics pipelines , 2012, Bioinform..
[7] Lior Pachter,et al. Near-optimal probabilistic RNA-seq quantification , 2016, Nature Biotechnology.
[8] Edgars Celms,et al. Variation in genomic landscape of clear cell renal cell carcinoma across Europe , 2014, Nature Communications.
[9] W. Huber,et al. which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. MAnorm: a robust model for quantitative comparison of ChIP-Seq data sets , 2011 .
[10] Rob Knight,et al. UCHIME improves sensitivity and speed of chimera detection , 2011, Bioinform..
[11] E. Mardis. The $1,000 genome, the $100,000 analysis? , 2010, Genome Medicine.
[12] Paul T. Groth,et al. The ENCODE (ENCyclopedia Of DNA Elements) Project , 2004, Science.
[13] F. Brimo,et al. Changes in the expression profiles of claudins during gonocyte differentiation and in seminomas , 2016, Andrology.
[14] Mathieu Blanchette,et al. BigDataScript: a scripting language for data pipelines , 2014, Bioinform..
[15] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[16] P. Laird,et al. Bis-SNP: Combined DNA methylation and SNP calling for Bisulfite-seq data , 2012, Genome Biology.
[17] Fabian A. Buske,et al. NGSANE: a lightweight production informatics framework for high-throughput data analysis , 2014, Bioinform..
[18] J. Mesirov,et al. GenePattern 2.0 , 2006, Nature Genetics.
[19] Michael Brudno,et al. Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations , 2014, Nature Genetics.
[20] Aaron A. Klammer,et al. Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data , 2013, Nature Methods.
[21] Brian D. O'Connor,et al. SeqWare Query Engine: storing and searching sequence data in the cloud , 2010, BMC Bioinformatics.
[22] R Redon,et al. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression , 2017, Molecular Psychiatry.
[23] Mauricio O. Carneiro,et al. From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline , 2013, Current protocols in bioinformatics.
[24] Chris Williams,et al. RNA-SeQC: RNA-seq metrics for quality control and process optimization , 2012, Bioinform..
[25] Paolo Di Tommaso,et al. Nextflow enables reproducible computational workflows , 2017, Nature Biotechnology.
[26] Måns Magnusson,et al. MultiQC: summarize analysis results for multiple tools and samples in a single report , 2016, Bioinform..
[27] Felix Krueger,et al. Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications , 2011, Bioinform..
[28] John Chilton,et al. The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2016 update , 2016, Nucleic Acids Res..
[29] Obi L. Griffith,et al. Informatics for RNA Sequencing: A Web Resource for Analysis on the Cloud , 2015, PLoS Comput. Biol..
[30] François Dubeau,et al. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. , 2017, American journal of human genetics.
[31] Philip A. Ewels,et al. HiCUP: pipeline for mapping and processing Hi-C data , 2015, F1000Research.
[32] Joshua M. Stuart,et al. Combining tumor genome simulation with crowdsourcing to benchmark somatic single-nucleotide-variant detection , 2015, Nature Methods.
[33] P. Buncic,et al. CernVM – a virtual software appliance for LHC applications , 2010 .
[34] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..
[35] Rob Knight,et al. PyNAST: a flexible tool for aligning sequences to a template alignment , 2009, Bioinform..
[36] Clifford A. Meyer,et al. Model-based Analysis of ChIP-Seq (MACS) , 2008, Genome Biology.
[37] Alexa B. R. McIntyre,et al. Extensive sequencing of seven human genomes to characterize benchmark reference materials , 2015, Scientific Data.
[38] Guillaume Bourque,et al. Identification of Elongated Primary Cilia with Impaired Mechanotransduction in Idiopathic Scoliosis Patients , 2017, Scientific Reports.
[39] Eric Talevich,et al. CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing , 2016, PLoS Comput. Biol..
[40] S. Oliver,et al. Estimating the total number of phosphoproteins and phosphorylation sites in eukaryotic proteomes , 2017, GigaScience.
[41] Mark D. Robinson,et al. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data , 2009, Bioinform..
[42] Jonathan M. Cairns,et al. CHiCAGO: robust detection of DNA looping interactions in Capture Hi-C data , 2015, Genome Biology.
[43] Paul Theodor Pyl,et al. HTSeq—a Python framework to work with high-throughput sequencing data , 2014, bioRxiv.
[44] Steven Salzberg,et al. BIOINFORMATICS ORIGINAL PAPER , 2004 .
[45] David G Hendrickson,et al. Differential analysis of gene regulation at transcript resolution with RNA-seq , 2012, Nature Biotechnology.
[46] Steven J. M. Jones,et al. The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery , 2016, Cell.
[47] Gary D Stormo,et al. An Overview of RNA Sequence Analyses: Structure Prediction, ncRNA Gene Identification, and RNAi Design , 2013, Current protocols in bioinformatics.
[48] Cole Trapnell,et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. , 2010, Nature biotechnology.
[49] Charles Shubert,et al. StarHPC — Teaching parallel programming within elastic compute cloud , 2009, Proceedings of the ITI 2009 31st International Conference on Information Technology Interfaces.
[50] Sven Rahmann,et al. Genome analysis , 2022 .
[51] Aaron R. Quinlan,et al. GEMINI: Integrative Exploration of Genetic Variation and Genome Annotations , 2013, PLoS Comput. Biol..
[52] E. Birney,et al. eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data , 2016, Cell reports.
[53] Christopher A. Miller,et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. , 2012, Genome research.
[54] Mark Gerstein,et al. MetaSV: an accurate and integrative structural-variant caller for next generation sequencing , 2015, Bioinform..
[55] Jacqueline A. Keane,et al. Circlator: automated circularization of genome assemblies using long sequencing reads , 2015, Genome Biology.
[56] Obi L. Griffith,et al. Genome Modeling System: A Knowledge Management Platform for Genomics , 2015, PLoS Comput. Biol..
[57] O. Hofmann,et al. VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research , 2016, Nucleic acids research.
[58] Adam P. Arkin,et al. FastTree: Computing Large Minimum Evolution Trees with Profiles instead of a Distance Matrix , 2009, Molecular biology and evolution.
[59] N. Friedman,et al. Trinity: reconstructing a full-length transcriptome without a genome from RNA-Seq data , 2011, Nature Biotechnology.
[60] Maxime Caron,et al. ERRα mediates metabolic adaptations driving lapatinib resistance in breast cancer , 2016, Nature Communications.
[61] Andrew I. Su,et al. Omics Pipe: a community-based framework for reproducible multi-omics data analysis , 2015, Bioinform..
[62] Thomas Zichner,et al. DELLY: structural variant discovery by integrated paired-end and split-read analysis , 2012, Bioinform..
[63] X. Zhou,et al. TopDom: an efficient and deterministic method for identifying topological domains in genomes , 2015, Nucleic acids research.
[64] E. Boerwinkle,et al. dbNSFP v3.0: A One‐Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice‐Site SNVs , 2016, Human mutation.
[65] Joachim Weischenfeldt,et al. SvABA: genome-wide detection of structural variants and indels by local assembly , 2018, Genome research.
[66] R. Redon,et al. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls , 2017, Neurobiology of Aging.
[67] Neva C. Durand,et al. Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments. , 2016, Cell systems.
[68] Guillaume Bourque,et al. Global characterization of copy number variants in epilepsy patients from whole genome sequencing , 2018, PLoS genetics.
[69] Mei Lu,et al. Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors. , 2016, Cancer cell.
[70] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[71] Matthew D. Young,et al. Gene ontology analysis for RNA-seq: accounting for selection bias , 2010, Genome Biology.
[72] Rob Knight,et al. Using QIIME to Analyze 16S rRNA Gene Sequences from Microbial Communities , 2011, Current protocols in bioinformatics.