Literature DB >> 23413434

Wessim: a whole-exome sequencing simulator based on in silico exome capture.

Sangwoo Kim1, Kyowon Jeong, Vineet Bafna.   

Abstract

SUMMARY: We propose a targeted re-sequencing simulator Wessim that generates synthetic exome sequencing reads from a given sample genome. Wessim emulates conventional exome capture technologies, including Agilent's SureSelect and NimbleGen's SeqCap, to generate DNA fragments from genomic target regions. The target regions can be either specified by genomic coordinates or inferred from in silico probe hybridization. Coupled with existing next-generation sequencing simulators, Wessim generates a realistic artificial exome sequencing data, which is essential for developing and evaluating exome-targeted variant callers. AVAILABILITY: Source code and the packaged version of Wessim with manuals are available at http://sak042.github.com/Wessim/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Mesh:

Year:  2013        PMID: 23413434      PMCID: PMC3624799          DOI: 10.1093/bioinformatics/btt074

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


  7 in total

1.  pIRS: Profile-based Illumina pair-end reads simulator.

Authors:  Xuesong Hu; Jianying Yuan; Yujian Shi; Jianliang Lu; Binghang Liu; Zhenyu Li; Yanxiang Chen; Desheng Mu; Hao Zhang; Nan Li; Zhen Yue; Fan Bai; Heng Li; Wei Fan
Journal:  Bioinformatics       Date:  2012-04-15       Impact factor: 6.937

2.  Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV.

Authors:  Jarupon Fah Sathirapongsasuti; Hane Lee; Basil A J Horst; Georg Brunner; Alistair J Cochran; Scott Binder; John Quackenbush; Stanley F Nelson
Journal:  Bioinformatics       Date:  2011-08-09       Impact factor: 6.937

3.  ART: a next-generation sequencing read simulator.

Authors:  Weichun Huang; Leping Li; Jason R Myers; Gabor T Marth
Journal:  Bioinformatics       Date:  2011-12-23       Impact factor: 6.937

4.  GemSIM: general, error-model based simulator of next-generation sequencing data.

Authors:  Kerensa E McElroy; Fabio Luciani; Torsten Thomas
Journal:  BMC Genomics       Date:  2012-02-15       Impact factor: 3.969

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.  Copy number variation detection and genotyping from exome sequence data.

Authors:  Niklas Krumm; Peter H Sudmant; Arthur Ko; Brian J O'Roak; Maika Malig; Bradley P Coe; Aaron R Quinlan; Deborah A Nickerson; Evan E Eichler
Journal:  Genome Res       Date:  2012-05-14       Impact factor: 9.043

7.  Summarizing and correcting the GC content bias in high-throughput sequencing.

Authors:  Yuval Benjamini; Terence P Speed
Journal:  Nucleic Acids Res       Date:  2012-02-09       Impact factor: 16.971

  7 in total
  14 in total

Review 1.  A broad survey of DNA sequence data simulation tools.

Authors:  Shatha Alosaimi; Armand Bandiang; Noelle van Biljon; Denis Awany; Prisca K Thami; Milaine S S Tchamga; Anmol Kiran; Olfa Messaoud; Radia Ismaeel Mohammed Hassan; Jacquiline Mugo; Azza Ahmed; Christian D Bope; Imane Allali; Gaston K Mazandu; Nicola J Mulder; Emile R Chimusa
Journal:  Brief Funct Genomics       Date:  2020-01-22       Impact factor: 4.241

2.  Structural variation and fusion detection using targeted sequencing data from circulating cell free DNA.

Authors:  Alexander R Gawroński; Yen-Yi Lin; Brian McConeghy; Stephane LeBihan; Hossein Asghari; Can Koçkan; Baraa Orabi; Nabil Adra; Roberto Pili; Colin C Collins; S Cenk Sahinalp; Faraz Hach
Journal:  Nucleic Acids Res       Date:  2019-04-23       Impact factor: 16.971

3.  SECNVs: A Simulator of Copy Number Variants and Whole-Exome Sequences From Reference Genomes.

Authors:  Yue Xing; Alan R Dabney; Xiao Li; Guosong Wang; Clare A Gill; Claudio Casola
Journal:  Front Genet       Date:  2020-02-21       Impact factor: 4.599

4.  cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.

Authors:  Evangelos Bellos; Vikrant Kumar; Clarabelle Lin; Jordi Maggi; Zai Yang Phua; Ching-Yu Cheng; Chui Ming Gemmy Cheung; Martin L Hibberd; Tien Yin Wong; Lachlan J M Coin; Sonia Davila
Journal:  Nucleic Acids Res       Date:  2014-09-16       Impact factor: 16.971

5.  Simulating Next-Generation Sequencing Datasets from Empirical Mutation and Sequencing Models.

Authors:  Zachary D Stephens; Matthew E Hudson; Liudmila S Mainzer; Morgan Taschuk; Matthew R Weber; Ravishankar K Iyer
Journal:  PLoS One       Date:  2016-11-28       Impact factor: 3.240

6.  ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data.

Authors:  Jinhwa Kong; Jaemoon Shin; Jungim Won; Keonbae Lee; Unjoo Lee; Jeehee Yoon
Journal:  Biomed Res Int       Date:  2017-06-18       Impact factor: 3.411

7.  Detailed simulation of cancer exome sequencing data reveals differences and common limitations of variant callers.

Authors:  Ariane L Hofmann; Jonas Behr; Jochen Singer; Jack Kuipers; Christian Beisel; Peter Schraml; Holger Moch; Niko Beerenwinkel
Journal:  BMC Bioinformatics       Date:  2017-01-03       Impact factor: 3.169

8.  Reliability of algorithmic somatic copy number alteration detection from targeted capture data.

Authors:  Nora Rieber; Regina Bohnert; Ulrike Ziehm; Gunther Jansen
Journal:  Bioinformatics       Date:  2017-09-15       Impact factor: 6.937

Review 9.  Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges.

Authors:  Biao Liu; Carl D Morrison; Candace S Johnson; Donald L Trump; Maochun Qin; Jeffrey C Conroy; Jianmin Wang; Song Liu
Journal:  Oncotarget       Date:  2013-11

10.  Comprehensive benchmarking of SNV callers for highly admixed tumor data.

Authors:  Regina Bohnert; Sonia Vivas; Gunther Jansen
Journal:  PLoS One       Date:  2017-10-11       Impact factor: 3.240

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