Source:http://linkedlifedata.com/resource/pubmed/id/21478487
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
|
pubmed:dateCreated |
2011-5-27
|
pubmed:abstractText |
Comrad is a novel algorithmic framework for the integrated analysis of RNA-Seq and whole genome shotgun sequencing (WGSS) data for the purposes of discovering genomic rearrangements and aberrant transcripts. The Comrad framework leverages the advantages of both RNA-Seq and WGSS data, providing accurate classification of rearrangements as expressed or not expressed and accurate classification of the genomic or non-genomic origin of aberrant transcripts. A major benefit of Comrad is its ability to accurately identify aberrant transcripts and associated rearrangements using low coverage genome data. As a result, a Comrad analysis can be performed at a cost comparable to that of two RNA-Seq experiments, significantly lower than an analysis requiring high coverage genome data.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1367-4811
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
1
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1481-8
|
pubmed:meshHeading |
pubmed-meshheading:21478487-Algorithms,
pubmed-meshheading:21478487-Cell Line, Tumor,
pubmed-meshheading:21478487-Chromosome Breakpoints,
pubmed-meshheading:21478487-Chromosome Mapping,
pubmed-meshheading:21478487-Gene Expression Profiling,
pubmed-meshheading:21478487-Gene Fusion,
pubmed-meshheading:21478487-Genomics,
pubmed-meshheading:21478487-Humans,
pubmed-meshheading:21478487-Mutant Chimeric Proteins,
pubmed-meshheading:21478487-RNA, Messenger,
pubmed-meshheading:21478487-RNA Splicing,
pubmed-meshheading:21478487-Sequence Analysis, DNA,
pubmed-meshheading:21478487-Sequence Analysis, RNA
|
pubmed:year |
2011
|
pubmed:articleTitle |
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
|
pubmed:affiliation |
School of Computing Science, Simon Fraser University, Burnaby, BC V5A 1S6, Canada. andrew.mcpherson@gmail.com
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|