Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/11568
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dc.contributor.authorTurro, E-
dc.contributor.authorSu, SY-
dc.contributor.authorGonçalves, A-
dc.contributor.authorCoin, LJM-
dc.contributor.authorRichardson, S-
dc.contributor.authorLewin, A-
dc.date.accessioned2015-11-09T14:02:13Z-
dc.date.available2011-02-10-
dc.date.available2015-11-09T14:02:13Z-
dc.date.issued2011-
dc.identifier.citationGenome Biology, 12:R13, (2011)en_US
dc.identifier.issn1474-7596-
dc.identifier.issn1474-760X-
dc.identifier.urihttp://www.genomebiology.com/2011/12/2/R13-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/11568-
dc.description.abstractWe present a novel pipeline and methodology for simultaneously estimating isoform expression and allelic imbalance in diploid organisms using RNA-seq data. We achieve this by modeling the expression of haplotype-specific isoforms. If unknown, the two parental isoform sequences can be individually reconstructed. A new statistical method, MMSEQ, deconvolves the mapping of reads to multiple transcripts (isoforms or haplotype-specific isoforms). Our software can take into account non-uniform read generation and works with paired-end reads.en_US
dc.description.sponsorshipBBSRC grant BBG0003521en_US
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.subjectIsoform level expressionen_US
dc.subjectRNA-seq dataen_US
dc.subjectMMSEQen_US
dc.titleHaplotype and isoform specific expression estimation using multi-mapping RNA-seq readsen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1186/gb-2011-12-2-r13-
dc.relation.isPartOfGenome Biology-
pubs.issue2-
pubs.volume12-
Appears in Collections:Dept of Mathematics Research Papers

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