Compression of Structured High-Throughput Sequencing Data

Large biological datasets are being produced at a rapid pace and create substantial storage challenges, particularly in the domain of high-throughput sequencing (HTS). Most approaches currently used to store HTS data are either unable to quickly adapt to the requirements of new sequencing or analysi...

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Bibliographic Details
Main Authors: Campagne, Fabien (Author), Dorff, Kevin C. (Author), Chambwe, Nyasha (Author), Robinson, James T. (Author), Mesirov, Jill P. (Contributor)
Other Authors: Koch Institute for Integrative Cancer Research at MIT (Contributor)
Format: Article
Language:English
Published: Public Library of Science, 2014-04-03T17:44:06Z.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Campagne, Fabien  |e author 
100 1 0 |a Koch Institute for Integrative Cancer Research at MIT  |e contributor 
100 1 0 |a Mesirov, Jill P.  |e contributor 
700 1 0 |a Dorff, Kevin C.  |e author 
700 1 0 |a Chambwe, Nyasha  |e author 
700 1 0 |a Robinson, James T.  |e author 
700 1 0 |a Mesirov, Jill P.  |e author 
245 0 0 |a Compression of Structured High-Throughput Sequencing Data 
260 |b Public Library of Science,   |c 2014-04-03T17:44:06Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/86000 
520 |a Large biological datasets are being produced at a rapid pace and create substantial storage challenges, particularly in the domain of high-throughput sequencing (HTS). Most approaches currently used to store HTS data are either unable to quickly adapt to the requirements of new sequencing or analysis methods (because they do not support schema evolution), or fail to provide state of the art compression of the datasets. We have devised new approaches to store HTS data that support seamless data schema evolution and compress datasets substantially better than existing approaches. Building on these new approaches, we discuss and demonstrate how a multi-tier data organization can dramatically reduce the storage, computational and network burden of collecting, analyzing, and archiving large sequencing datasets. For instance, we show that spliced RNA-Seq alignments can be stored in less than 4% the size of a BAM file with perfect data fidelity. Compared to the previous compression state of the art, these methods reduce dataset size more than 40% when storing exome, gene expression or DNA methylation datasets. The approaches have been integrated in a comprehensive suite of software tools (http://goby.campagnelab.org) that support common analyses for a range of high-throughput sequencing assays. 
520 |a National Center for Research Resources (U.S.) (Grant UL1 RR024996) 
520 |a Leukemia & Lymphoma Society of America (Translational Research Program Grant LLS 6304-11) 
520 |a National Institute of Mental Health (U.S.) (R01 MH086883) 
546 |a en_US 
655 7 |a Article 
773 |t PLoS ONE