Varlociraptor: enhancing sensitivity and controlling false discovery rate in somatic indel discovery
暂无分享,去创建一个
Alexander Schönhuth | Tobias Marschall | Johannes Köster | T. Marschall | A. Schönhuth | Louis J. Dijkstra | L. Dijkstra | Johannes Köster
[1] Heng Li,et al. A survey of sequence alignment algorithms for next-generation sequencing , 2010, Briefings Bioinform..
[2] Marc J. Williams,et al. Identification of neutral tumor evolution across cancer types , 2016, Nature Genetics.
[3] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[4] Timothy B. Stockwell,et al. The Diploid Genome Sequence of an Individual Human , 2007, PLoS biology.
[5] C. Robert,et al. Optimal Sample Size for Multiple Testing : the Case of Gene Expression Mi roarraysPeter , 2004 .
[6] T. Speed,et al. GRIDSS: sensitive and specific genomic rearrangement detection using positional de Bruijn graph assembly. , 2017, Genome research.
[7] Steven J. M. Jones,et al. A somatic reference standard for cancer genome sequencing , 2016, Scientific Reports.
[8] S. Phinn,et al. Australian vegetated coastal ecosystems as global hotspots for climate change mitigation , 2019, Nature Communications.
[9] Alexander Zelikovsky,et al. Computational Methods for Next Generation Sequencing Data Analysis , 2016 .
[10] Vladimir Vacic,et al. Genome-wide somatic variant calling using localized colored de Bruijn graphs , 2018, Communications Biology.
[11] Heng Li,et al. Toward better understanding of artifacts in variant calling from high-coverage samples , 2014, Bioinform..
[12] Nuno A. Fonseca,et al. Assemblathon 1: a competitive assessment of de novo short read assembly methods. , 2011, Genome research.
[13] W. Xiao,et al. Robust Cancer Mutation Detection with Deep Learning Models Derived from Tumor-Normal Sequencing Data , 2019, bioRxiv.
[14] Y. Kamatani,et al. Comprehensive evaluation of structural variation detection algorithms for whole genome sequencing , 2019, Genome Biology.
[15] N. McGranahan,et al. The causes and consequences of genetic heterogeneity in cancer evolution , 2013, Nature.
[16] James T. Robinson,et al. Variant Review with the Integrative Genomics Viewer. , 2017, Cancer research.
[17] Durbin,et al. Biological Sequence Analysis , 1998 .
[18] Xiaoyu Chen,et al. Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications , 2016, Bioinform..
[19] Gary D Bader,et al. International network of cancer genome projects , 2010, Nature.
[20] Gabor T. Marth,et al. Haplotype-based variant detection from short-read sequencing , 2012, 1207.3907.
[21] klaguia. International Network of Cancer Genome Projects , 2010 .
[22] Hugo Y. K. Lam,et al. Deep convolutional neural networks for accurate somatic mutation detection , 2018, Nature Communications.
[23] Iman Hajirasouliha,et al. MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels , 2013, Bioinform..
[24] Heng Li. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.
[25] Alexander Schönhuth,et al. Repeat- and error-aware comparison of deletions , 2015, Bioinform..
[26] Thomas Zichner,et al. DELLY: structural variant discovery by integrated paired-end and split-read analysis , 2012, Bioinform..
[27] P. Müller,et al. Optimal Sample Size for Multiple Testing , 2004 .
[28] Lars Arvestad,et al. Structural Variation Detection with Read Pair Information: An Improved Null Hypothesis Reduces Bias , 2017, J. Comput. Biol..
[29] Knut Reinert,et al. Gustaf: Detecting and correctly classifying SVs in the NGS twilight zone , 2014, Bioinform..
[30] Ryan M. Layer,et al. LUMPY: a probabilistic framework for structural variant discovery , 2012, Genome Biology.
[31] Michael C. Heinold,et al. A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing , 2015, Nature Communications.
[32] James O. Berger,et al. Modularization in Bayesian analysis, with emphasis on analysis of computer models , 2009 .
[33] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[34] Joshua M. Stuart,et al. The Cancer Genome Atlas Pan-Cancer analysis project , 2013, Nature Genetics.
[35] L. Ding,et al. novoBreak: local assembly for breakpoint detection in cancer genomes , 2016, Nature Methods.
[36] Giulia Galotto,et al. Unique Molecular Identifiers reveal a novel sequencing artefact with implications for RNA-Seq based gene expression analysis , 2018, Scientific Reports.
[37] Alexander Schliep,et al. CLEVER: clique-enumerating variant finder , 2012, Bioinform..
[38] Jay Shendure,et al. Classification and characterization of microsatellite instability across 18 cancer types , 2016, Nature Medicine.
[39] Alexandre Z. Caldeira,et al. Uncertainty in homology inferences: assessing and improving genomic sequence alignment. , 2008, Genome research.
[40] Weitai Huang,et al. SMuRF: portable and accurate ensemble prediction of somatic mutations , 2019, Bioinform..
[41] Mauricio O. Carneiro,et al. Scaling accurate genetic variant discovery to tens of thousands of samples , 2017, bioRxiv.
[42] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[43] Benjamin Neale,et al. A synthetic-diploid benchmark for accurate variant calling evaluation , 2018, Nature Methods.
[44] A. Sivachenko,et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples , 2013, Nature Biotechnology.
[45] Sven Rahmann,et al. Genome analysis , 2022 .
[46] Wendy S. W. Wong,et al. Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs , 2012, Bioinform..
[47] Renan Valieris,et al. Bioconda: sustainable and comprehensive software distribution for the life sciences , 2018, Nature Methods.
[48] Eugene W. Myers,et al. A fast bit-vector algorithm for approximate string matching based on dynamic programming , 1998, JACM.
[49] M. DePristo,et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data , 2011, Nature Genetics.
[50] Gad Getz,et al. Analysis of somatic microsatellite indels identifies driver events in human tumors , 2017, Nature Biotechnology.
[51] Sven Rahmann,et al. Snakemake--a scalable bioinformatics workflow engine. , 2012, Bioinformatics.
[52]
R. Durbin,et al.
Mapping Quality Scores Mapping Short Dna Sequencing Reads and Calling Variants Using P ,
2022
.
[53]
Alexander Schönhuth,et al.
Discovering motifs that induce sequencing errors
,
2013,
BMC Bioinformatics.