Literature DB >> 24618469

pRESTO: a toolkit for processing high-throughput sequencing raw reads of lymphocyte receptor repertoires.

Jason A Vander Heiden1, Gur Yaari2, Mohamed Uduman2, Joel N H Stern3, Kevin C O'Connor2, David A Hafler2, Francois Vigneault1, Steven H Kleinstein2.   

Abstract

UNLABELLED: Driven by dramatic technological improvements, large-scale characterization of lymphocyte receptor repertoires via high-throughput sequencing is now feasible. Although promising, the high germline and somatic diversity, especially of B-cell immunoglobulin repertoires, presents challenges for analysis requiring the development of specialized computational pipelines. We developed the REpertoire Sequencing TOolkit (pRESTO) for processing reads from high-throughput lymphocyte receptor studies. pRESTO processes raw sequences to produce error-corrected, sorted and annotated sequence sets, along with a wealth of metrics at each step. The toolkit supports multiplexed primer pools, single- or paired-end reads and emerging technologies that use single-molecule identifiers. pRESTO has been tested on data generated from Roche and Illumina platforms. It has a built-in capacity to parallelize the work between available processors and is able to efficiently process millions of sequences generated by typical high-throughput projects.
AVAILABILITY AND IMPLEMENTATION: pRESTO is freely available for academic use. The software package and detailed tutorials may be downloaded from http://clip.med.yale.edu/presto.
© 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: 24618469      PMCID: PMC4071206          DOI: 10.1093/bioinformatics/btu138

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


  12 in total

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  160 in total

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5.  Automated analysis of high-throughput B-cell sequencing data reveals a high frequency of novel immunoglobulin V gene segment alleles.

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6.  The mutation patterns in B-cell immunoglobulin receptors reflect the influence of selection acting at multiple time-scales.

Authors:  Gur Yaari; Jennifer I C Benichou; Jason A Vander Heiden; Steven H Kleinstein; Yoram Louzoun
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7.  Phylogenetic analysis of the human antibody repertoire reveals quantitative signatures of immune senescence and aging.

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9.  Lack of Evidence for a Substantial Rate of Templated Mutagenesis in B Cell Diversification.

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10.  Neutralizing antibodies against West Nile virus identified directly from human B cells by single-cell analysis and next generation sequencing.

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Journal:  Integr Biol (Camb)       Date:  2015-10-20       Impact factor: 2.192

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