Literature DB >> 28011768

SeqLib: a C ++ API for rapid BAM manipulation, sequence alignment and sequence assembly.

Jeremiah Wala1,2,3, Rameen Beroukhim1,2,3.   

Abstract

We present SeqLib, a C ++ API and command line tool that provides a rapid and user-friendly interface to BAM/SAM/CRAM files, global sequence alignment operations and sequence assembly. Four C libraries perform core operations in SeqLib: HTSlib for BAM access, BWA-MEM and BLAT for sequence alignment and Fermi for error correction and sequence assembly. Benchmarking indicates that SeqLib has lower CPU and memory requirements than leading C ++ sequence analysis APIs. We demonstrate an example of how minimal SeqLib code can extract, error-correct and assemble reads from a CRAM file and then align with BWA-MEM. SeqLib also provides additional capabilities, including chromosome-aware interval queries and read plotting. Command line tools are available for performing integrated error correction, micro-assemblies and alignment. Availability and Implementation: SeqLib is available on Linux and OSX for the C ++98 standard and later at github.com/walaj/SeqLib. SeqLib is released under the Apache2 license. Additional capabilities for BLAT alignment are available under the BLAT license. Contact: jwala@broadinstitue.org ; rameen@broadinstitute.org.
© The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com

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Year:  2017        PMID: 28011768      PMCID: PMC5859992          DOI: 10.1093/bioinformatics/btw741

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


  6 in total

1.  BLAT--the BLAST-like alignment tool.

Authors:  W James Kent
Journal:  Genome Res       Date:  2002-04       Impact factor: 9.043

2.  Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2012-05-07       Impact factor: 6.937

3.  BamTools: a C++ API and toolkit for analyzing and managing BAM files.

Authors:  Derek W Barnett; Erik K Garrison; Aaron R Quinlan; Michael P Strömberg; Gabor T Marth
Journal:  Bioinformatics       Date:  2011-04-14       Impact factor: 6.937

4.  BFC: correcting Illumina sequencing errors.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2015-05-06       Impact factor: 6.937

5.  VariantBam: filtering and profiling of next-generational sequencing data using region-specific rules.

Authors:  Jeremiah Wala; Cheng-Zhong Zhang; Matthew Meyerson; Rameen Beroukhim
Journal:  Bioinformatics       Date:  2016-02-26       Impact factor: 6.937

6.  SeqAn an efficient, generic C++ library for sequence analysis.

Authors:  Andreas Döring; David Weese; Tobias Rausch; Knut Reinert
Journal:  BMC Bioinformatics       Date:  2008-01-09       Impact factor: 3.169

  6 in total
  4 in total

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Authors:  Jeremiah A Wala; Pratiti Bandopadhayay; Noah F Greenwald; Ryan O'Rourke; Ted Sharpe; Chip Stewart; Steve Schumacher; Yilong Li; Joachim Weischenfeldt; Xiaotong Yao; Chad Nusbaum; Peter Campbell; Gad Getz; Matthew Meyerson; Cheng-Zhong Zhang; Marcin Imielinski; Rameen Beroukhim
Journal:  Genome Res       Date:  2018-03-13       Impact factor: 9.438

2.  Structural variant evolution after telomere crisis.

Authors:  Sally M Dewhurst; Xiaotong Yao; Joel Rosiene; Huasong Tian; Julie Behr; Nazario Bosco; Kaori K Takai; Titia de Lange; Marcin Imieliński
Journal:  Nat Commun       Date:  2021-04-07       Impact factor: 14.919

3.  RNA-SeQC 2: Efficient RNA-seq quality control and quantification for large cohorts.

Authors:  Aaron Graubert; François Aguet; Arvind Ravi; Kristin G Ardlie; Gad Getz
Journal:  Bioinformatics       Date:  2021-03-02       Impact factor: 6.937

4.  NPSV: A simulation-driven approach to genotyping structural variants in whole-genome sequencing data.

Authors:  Michael D Linderman; Crystal Paudyal; Musab Shakeel; William Kelley; Ali Bashir; Bruce D Gelb
Journal:  Gigascience       Date:  2021-07-01       Impact factor: 6.524

  4 in total

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