Literature DB >> 24894505

SMaSH: a benchmarking toolkit for human genome variant calling.

Ameet Talwalkar1, Jesse Liptrap1, Julie Newcomb1, Christopher Hartl2, Jonathan Terhorst1, Kristal Curtis1, Ma'ayan Bresler1, Yun S Song2, Michael I Jordan2, David Patterson1.   

Abstract

MOTIVATION: Computational methods are essential to extract actionable information from raw sequencing data, and to thus fulfill the promise of next-generation sequencing technology. Unfortunately, computational tools developed to call variants from human sequencing data disagree on many of their predictions, and current methods to evaluate accuracy and computational performance are ad hoc and incomplete. Agreement on benchmarking variant calling methods would stimulate development of genomic processing tools and facilitate communication among researchers.
RESULTS: We propose SMaSH, a benchmarking methodology for evaluating germline variant calling algorithms. We generate synthetic datasets, organize and interpret a wide range of existing benchmarking data for real genomes and propose a set of accuracy and computational performance metrics for evaluating variant calling methods on these benchmarking data. Moreover, we illustrate the utility of SMaSH to evaluate the performance of some leading single-nucleotide polymorphism, indel and structural variant calling algorithms.
AVAILABILITY AND IMPLEMENTATION: We provide free and open access online to the SMaSH tool kit, along with detailed documentation, at smash.cs.berkeley.edu
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2014        PMID: 24894505      PMCID: PMC4173010          DOI: 10.1093/bioinformatics/btu345

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  19 in total

1.  High-quality draft assemblies of mammalian genomes from massively parallel sequence data.

Authors:  Sante Gnerre; Iain Maccallum; Dariusz Przybylski; Filipe J Ribeiro; Joshua N Burton; Bruce J Walker; Ted Sharpe; Giles Hall; Terrance P Shea; Sean Sykes; Aaron M Berlin; Daniel Aird; Maura Costello; Riza Daza; Louise Williams; Robert Nicol; Andreas Gnirke; Chad Nusbaum; Eric S Lander; David B Jaffe
Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-27       Impact factor: 11.205

Review 2.  Next-generation sequencing data interpretation: enhancing reproducibility and accessibility.

Authors:  Anton Nekrutenko; James Taylor
Journal:  Nat Rev Genet       Date:  2012-09       Impact factor: 53.242

3.  Assemblathon 1: a competitive assessment of de novo short read assembly methods.

Authors:  Dent Earl; Keith Bradnam; John St John; Aaron Darling; Dawei Lin; Joseph Fass; Hung On Ken Yu; Vince Buffalo; Daniel R Zerbino; Mark Diekhans; Ngan Nguyen; Pramila Nuwantha Ariyaratne; Wing-Kin Sung; Zemin Ning; Matthias Haimel; Jared T Simpson; Nuno A Fonseca; İnanç Birol; T Roderick Docking; Isaac Y Ho; Daniel S Rokhsar; Rayan Chikhi; Dominique Lavenier; Guillaume Chapuis; Delphine Naquin; Nicolas Maillet; Michael C Schatz; David R Kelley; Adam M Phillippy; Sergey Koren; Shiaw-Pyng Yang; Wei Wu; Wen-Chi Chou; Anuj Srivastava; Timothy I Shaw; J Graham Ruby; Peter Skewes-Cox; Miguel Betegon; Michelle T Dimon; Victor Solovyev; Igor Seledtsov; Petr Kosarev; Denis Vorobyev; Ricardo Ramirez-Gonzalez; Richard Leggett; Dan MacLean; Fangfang Xia; Ruibang Luo; Zhenyu Li; Yinlong Xie; Binghang Liu; Sante Gnerre; Iain MacCallum; Dariusz Przybylski; Filipe J Ribeiro; Shuangye Yin; Ted Sharpe; Giles Hall; Paul J Kersey; Richard Durbin; Shaun D Jackman; Jarrod A Chapman; Xiaoqiu Huang; Joseph L DeRisi; Mario Caccamo; Yingrui Li; David B Jaffe; Richard E Green; David Haussler; Ian Korf; Benedict Paten
Journal:  Genome Res       Date:  2011-09-16       Impact factor: 9.043

4.  Integrating common and rare genetic variation in diverse human populations.

Authors:  David M Altshuler; Richard A Gibbs; Leena Peltonen; David M Altshuler; Richard A Gibbs; Leena Peltonen; Emmanouil Dermitzakis; Stephen F Schaffner; Fuli Yu; Leena Peltonen; Emmanouil Dermitzakis; Penelope E Bonnen; David M Altshuler; Richard A Gibbs; Paul I W de Bakker; Panos Deloukas; Stacey B Gabriel; Rhian Gwilliam; Sarah Hunt; Michael Inouye; Xiaoming Jia; Aarno Palotie; Melissa Parkin; Pamela Whittaker; Fuli Yu; Kyle Chang; Alicia Hawes; Lora R Lewis; Yanru Ren; David Wheeler; Richard A Gibbs; Donna Marie Muzny; Chris Barnes; Katayoon Darvishi; Matthew Hurles; Joshua M Korn; Kati Kristiansson; Charles Lee; Steven A McCarrol; James Nemesh; Emmanouil Dermitzakis; Alon Keinan; Stephen B Montgomery; Samuela Pollack; Alkes L Price; Nicole Soranzo; Penelope E Bonnen; Richard A Gibbs; Claudia Gonzaga-Jauregui; Alon Keinan; Alkes L Price; Fuli Yu; Verneri Anttila; Wendy Brodeur; Mark J Daly; Stephen Leslie; Gil McVean; Loukas Moutsianas; Huy Nguyen; Stephen F Schaffner; Qingrun Zhang; Mohammed J R Ghori; Ralph McGinnis; William McLaren; Samuela Pollack; Alkes L Price; Stephen F Schaffner; Fumihiko Takeuchi; Sharon R Grossman; Ilya Shlyakhter; Elizabeth B Hostetter; Pardis C Sabeti; Clement A Adebamowo; Morris W Foster; Deborah R Gordon; Julio Licinio; Maria Cristina Manca; Patricia A Marshall; Ichiro Matsuda; Duncan Ngare; Vivian Ota Wang; Deepa Reddy; Charles N Rotimi; Charmaine D Royal; Richard R Sharp; Changqing Zeng; Lisa D Brooks; Jean E McEwen
Journal:  Nature       Date:  2010-09-02       Impact factor: 49.962

5.  The Sequence Alignment/Map format and SAMtools.

Authors:  Heng Li; Bob Handsaker; Alec Wysoker; Tim Fennell; Jue Ruan; Nils Homer; Gabor Marth; Goncalo Abecasis; Richard Durbin
Journal:  Bioinformatics       Date:  2009-06-08       Impact factor: 6.937

6.  Characterization of missing human genome sequences and copy-number polymorphic insertions.

Authors:  Jeffrey M Kidd; Nick Sampas; Francesca Antonacci; Tina Graves; Robert Fulton; Hillary S Hayden; Can Alkan; Maika Malig; Mario Ventura; Giuliana Giannuzzi; Joelle Kallicki; Paige Anderson; Anya Tsalenko; N Alice Yamada; Peter Tsang; Rajinder Kaul; Richard K Wilson; Laurakay Bruhn; Evan E Eichler
Journal:  Nat Methods       Date:  2010-05       Impact factor: 28.547

7.  A second generation human haplotype map of over 3.1 million SNPs.

Authors:  Kelly A Frazer; Dennis G Ballinger; David R Cox; David A Hinds; Laura L Stuve; Richard A Gibbs; John W Belmont; Andrew Boudreau; Paul Hardenbol; Suzanne M Leal; Shiran Pasternak; David A Wheeler; Thomas D Willis; Fuli Yu; Huanming Yang; Changqing Zeng; Yang Gao; Haoran Hu; Weitao Hu; Chaohua Li; Wei Lin; Siqi Liu; Hao Pan; Xiaoli Tang; Jian Wang; Wei Wang; Jun Yu; Bo Zhang; Qingrun Zhang; Hongbin Zhao; Hui Zhao; Jun Zhou; Stacey B Gabriel; Rachel Barry; Brendan Blumenstiel; Amy Camargo; Matthew Defelice; Maura Faggart; Mary Goyette; Supriya Gupta; Jamie Moore; Huy Nguyen; Robert C Onofrio; Melissa Parkin; Jessica Roy; Erich Stahl; Ellen Winchester; Liuda Ziaugra; David Altshuler; Yan Shen; Zhijian Yao; Wei Huang; Xun Chu; Yungang He; Li Jin; Yangfan Liu; Yayun Shen; Weiwei Sun; Haifeng Wang; Yi Wang; Ying Wang; Xiaoyan Xiong; Liang Xu; Mary M Y Waye; Stephen K W Tsui; Hong Xue; J Tze-Fei Wong; Luana M Galver; Jian-Bing Fan; Kevin Gunderson; Sarah S Murray; Arnold R Oliphant; Mark S Chee; Alexandre Montpetit; Fanny Chagnon; Vincent Ferretti; Martin Leboeuf; Jean-François Olivier; Michael S Phillips; Stéphanie Roumy; Clémentine Sallée; Andrei Verner; Thomas J Hudson; Pui-Yan Kwok; Dongmei Cai; Daniel C Koboldt; Raymond D Miller; Ludmila Pawlikowska; Patricia Taillon-Miller; Ming Xiao; Lap-Chee Tsui; William Mak; You Qiang Song; Paul K H Tam; Yusuke Nakamura; Takahisa Kawaguchi; Takuya Kitamoto; Takashi Morizono; Atsushi Nagashima; Yozo Ohnishi; Akihiro Sekine; Toshihiro Tanaka; Tatsuhiko Tsunoda; Panos Deloukas; Christine P Bird; Marcos Delgado; Emmanouil T Dermitzakis; Rhian Gwilliam; Sarah Hunt; Jonathan Morrison; Don Powell; Barbara E Stranger; Pamela Whittaker; David R Bentley; Mark J Daly; Paul I W de Bakker; Jeff Barrett; Yves R Chretien; Julian Maller; Steve McCarroll; Nick Patterson; Itsik Pe'er; Alkes Price; Shaun Purcell; Daniel J Richter; Pardis Sabeti; Richa Saxena; Stephen F Schaffner; Pak C Sham; Patrick Varilly; David Altshuler; Lincoln D Stein; Lalitha Krishnan; Albert Vernon Smith; Marcela K Tello-Ruiz; Gudmundur A Thorisson; Aravinda Chakravarti; Peter E Chen; David J Cutler; Carl S Kashuk; Shin Lin; Gonçalo R Abecasis; Weihua Guan; Yun Li; Heather M Munro; Zhaohui Steve Qin; Daryl J Thomas; Gilean McVean; Adam Auton; Leonardo Bottolo; Niall Cardin; Susana Eyheramendy; Colin Freeman; Jonathan Marchini; Simon Myers; Chris Spencer; Matthew Stephens; Peter Donnelly; Lon R Cardon; Geraldine Clarke; David M Evans; Andrew P Morris; Bruce S Weir; Tatsuhiko Tsunoda; James C Mullikin; Stephen T Sherry; Michael Feolo; Andrew Skol; Houcan Zhang; Changqing Zeng; Hui Zhao; Ichiro Matsuda; Yoshimitsu Fukushima; Darryl R Macer; Eiko Suda; Charles N Rotimi; Clement A Adebamowo; Ike Ajayi; Toyin Aniagwu; Patricia A Marshall; Chibuzor Nkwodimmah; Charmaine D M Royal; Mark F Leppert; Missy Dixon; Andy Peiffer; Renzong Qiu; Alastair Kent; Kazuto Kato; Norio Niikawa; Isaac F Adewole; Bartha M Knoppers; Morris W Foster; Ellen Wright Clayton; Jessica Watkin; Richard A Gibbs; John W Belmont; Donna Muzny; Lynne Nazareth; Erica Sodergren; George M Weinstock; David A Wheeler; Imtaz Yakub; Stacey B Gabriel; Robert C Onofrio; Daniel J Richter; Liuda Ziaugra; Bruce W Birren; Mark J Daly; David Altshuler; Richard K Wilson; Lucinda L Fulton; Jane Rogers; John Burton; Nigel P Carter; Christopher M Clee; Mark Griffiths; Matthew C Jones; Kirsten McLay; Robert W Plumb; Mark T Ross; Sarah K Sims; David L Willey; Zhu Chen; Hua Han; Le Kang; Martin Godbout; John C Wallenburg; Paul L'Archevêque; Guy Bellemare; Koji Saeki; Hongguang Wang; Daochang An; Hongbo Fu; Qing Li; Zhen Wang; Renwu Wang; Arthur L Holden; Lisa D Brooks; Jean E McEwen; Mark S Guyer; Vivian Ota Wang; Jane L Peterson; Michael Shi; Jack Spiegel; Lawrence M Sung; Lynn F Zacharia; Francis S Collins; Karen Kennedy; Ruth Jamieson; John Stewart
Journal:  Nature       Date:  2007-10-18       Impact factor: 49.962

8.  A human genome structural variation sequencing resource reveals insights into mutational mechanisms.

Authors:  Jeffrey M Kidd; Tina Graves; Tera L Newman; Robert Fulton; Hillary S Hayden; Maika Malig; Joelle Kallicki; Rajinder Kaul; Richard K Wilson; Evan E Eichler
Journal:  Cell       Date:  2010-11-24       Impact factor: 41.582

9.  A framework for variation discovery and genotyping using next-generation DNA sequencing data.

Authors:  Mark A DePristo; Eric Banks; Ryan Poplin; Kiran V Garimella; Jared R Maguire; Christopher Hartl; Anthony A Philippakis; Guillermo del Angel; Manuel A Rivas; Matt Hanna; Aaron McKenna; Tim J Fennell; Andrew M Kernytsky; Andrey Y Sivachenko; Kristian Cibulskis; Stacey B Gabriel; David Altshuler; Mark J Daly
Journal:  Nat Genet       Date:  2011-04-10       Impact factor: 38.330

10.  The diploid genome sequence of an individual human.

Authors:  Samuel Levy; Granger Sutton; Pauline C Ng; Lars Feuk; Aaron L Halpern; Brian P Walenz; Nelson Axelrod; Jiaqi Huang; Ewen F Kirkness; Gennady Denisov; Yuan Lin; Jeffrey R MacDonald; Andy Wing Chun Pang; Mary Shago; Timothy B Stockwell; Alexia Tsiamouri; Vineet Bafna; Vikas Bansal; Saul A Kravitz; Dana A Busam; Karen Y Beeson; Tina C McIntosh; Karin A Remington; Josep F Abril; John Gill; Jon Borman; Yu-Hui Rogers; Marvin E Frazier; Stephen W Scherer; Robert L Strausberg; J Craig Venter
Journal:  PLoS Biol       Date:  2007-09-04       Impact factor: 8.029

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  19 in total

1.  Jointly aligning a group of DNA reads improves accuracy of identifying large deletions.

Authors:  Anish M S Shrestha; Martin C Frith; Kiyoshi Asai; Hugues Richard
Journal:  Nucleic Acids Res       Date:  2018-02-16       Impact factor: 16.971

Review 2.  Toward better understanding of artifacts in variant calling from high-coverage samples.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2014-06-27       Impact factor: 6.937

3.  An Evaluation Framework for Lossy Compression of Genome Sequencing Quality Values.

Authors:  Claudio Alberti; Noah Daniels; Mikel Hernaez; Jan Voges; Rachel L Goldfeder; Ana A Hernandez-Lopez; Marco Mattavelli; Bonnie Berger
Journal:  Proc Data Compress Conf       Date:  2016-12-19

Review 4.  Transposable element detection from whole genome sequence data.

Authors:  Adam D Ewing
Journal:  Mob DNA       Date:  2015-12-29

5.  Comparing complex variants in family trios.

Authors:  Berke Ç Toptas; Goran Rakocevic; Péter Kómár; Deniz Kural
Journal:  Bioinformatics       Date:  2018-12-15       Impact factor: 6.937

6.  VarSim: a high-fidelity simulation and validation framework for high-throughput genome sequencing with cancer applications.

Authors:  John C Mu; Marghoob Mohiyuddin; Jian Li; Narges Bani Asadi; Mark B Gerstein; Alexej Abyzov; Wing H Wong; Hugo Y K Lam
Journal:  Bioinformatics       Date:  2014-12-17       Impact factor: 6.937

7.  An analytical framework for optimizing variant discovery from personal genomes.

Authors:  Gareth Highnam; Jason J Wang; Dean Kusler; Justin Zook; Vinaya Vijayan; Nir Leibovich; David Mittelman
Journal:  Nat Commun       Date:  2015-02-25       Impact factor: 14.919

Review 8.  Best practices for evaluating single nucleotide variant calling methods for microbial genomics.

Authors:  Nathan D Olson; Steven P Lund; Rebecca E Colman; Jeffrey T Foster; Jason W Sahl; James M Schupp; Paul Keim; Jayne B Morrow; Marc L Salit; Justin M Zook
Journal:  Front Genet       Date:  2015-07-07       Impact factor: 4.599

9.  A call for benchmarking transposable element annotation methods.

Authors:  Douglas R Hoen; Glenn Hickey; Guillaume Bourque; Josep Casacuberta; Richard Cordaux; Cédric Feschotte; Anna-Sophie Fiston-Lavier; Aurélie Hua-Van; Robert Hubley; Aurélie Kapusta; Emmanuelle Lerat; Florian Maumus; David D Pollock; Hadi Quesneville; Arian Smit; Travis J Wheeler; Thomas E Bureau; Mathieu Blanchette
Journal:  Mob DNA       Date:  2015-08-04

Review 10.  Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.

Authors:  Riyue Bao; Lei Huang; Jorge Andrade; Wei Tan; Warren A Kibbe; Hongmei Jiang; Gang Feng
Journal:  Cancer Inform       Date:  2014-09-21
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