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From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline

G. Van der Auwera, M. Carneiro, C. Hartl, R. Poplin, G. Del Angel, A. Levy-Moonshine, T. Jordan, K. Shakir, D. Roazen, J. Thibault, E. Banks, K. Garimella, D. Altshuler, S. Gabriel, and M. DePristo. Curr Protoc Bioinformatics, (2013)
DOI: 10.1002/0471250953.bi1110s43

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S Fröhlich

S Ulrich

S Bachmann

S Hilt

S Steinlechner

Other publications of authors with the same name

A second generation human haplotype map of over 3.1 million SNPsInternational HapMap Consortium, K. Frazer, D. Ballinger, D. Cox, D. Hinds, L. Stuve, R. Gibbs, J. Belmont, A. Boudreau, P. Hardenbol and 241 other author(s). Nature, 449 (7164): 851-861 (October 2007)Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolutionS. Kasar, J. Kim, R. Improgo, G. Tiao, P. Polak, N. Haradhvala, M. Lawrence, A. Kiezun, S. Fernandes, S. Bahl and 6 other author(s). Nature Communications, (December 2015)Genomic correlates of response to CTLA-4 blockade in metastatic melanomaE. Van Allen, D. Miao, B. Schilling, S. Shukla, C. Blank, L. Zimmer, A. Sucker, U. Hillen, M. Foppen, S. Goldinger and 12 other author(s). Science, 350 (6257): 207-211 (October 2015)From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipelineG. Van der Auwera, M. Carneiro, C. Hartl, R. Poplin, G. Del Angel, A. Levy-Moonshine, T. Jordan, K. Shakir, D. Roazen, J. Thibault and 5 other author(s). Curr Protoc Bioinformatics, (2013)Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human ExomesJ. Tennessen, A. Bigham, T. O'Connor, W. Fu, E. Kenny, S. Gravel, S. McGee, R. Do, X. Liu, G. Jun and 16 other author(s). Science, (May 2012)Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicineE. Van Allen, N. Wagle, P. Stojanov, D. Perrin, K. Cibulskis, S. Marlow, J. Jane-Valbuena, D. Friedrich, G. Kryukov, S. Carter and 26 other author(s). Nat Med, 20 (6): 682-688 (June 2014)Whole-genome and multisector exome sequencing of primary and post-treatment glioblastoma reveals patterns of tumor evolutionH. Kim, S. Zheng, S. Amini, S. Virk, T. Mikkelsen, D. Brat, J. Grimsby, C. Sougnez, F. Muller, J. Hu and 13 other author(s). Genome Res, 25 (3): 316-327 (March 2015)The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing dataA. McKenna, M. Hanna, E. Banks, A. Sivachenko, K. Cibulskis, A. Kernytsky, K. Garimella, D. Altshuler, S. Gabriel, M. Daly and 1 other author(s). Genome Res, 20 (9): 1297-1303 (September 2010)A scalable, fully automated process for construction of sequence-ready human exome targeted capture librariesS. Fisher, A. Barry, J. Abreu, B. Minie, J. Nolan, T. Delorey, G. Young, T. Fennell, A. Allen, L. Ambrogio and 17 other author(s). Genome Biol, (2011)Cost-consequence analysis in a French setting of screening and optimal treatment of nephropathy in hypertensive patients with type 2 diabetes.A. Palmer, R. Chen, W. Valentine, S. Roze, B. Bregman, N. Mehin, and S. Gabriel. (xx 02 2006)

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Disambiguation of "Gabriel, S"

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From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline

Please choose a person to relate this publication to

S Fröhlich

S Ulrich

S Bachmann

S Hilt

S Steinlechner

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Gabriel, S"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline

Please choose a person to relate this publication to

S Fröhlich

S Ulrich

S Bachmann

S Hilt

S Steinlechner

Other publications of authors with the same name

Disambiguation

copy delete add this publication to your clipboard
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URL
DOI
BibTeX
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Chicago
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From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline