TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-04-25

AUTHORS

Daehwan Kim, Geo Pertea, Cole Trapnell, Harold Pimentel, Ryan Kelley, Steven L Salzberg

ABSTRACT

TopHat is a popular spliced aligner for RNA-sequence (RNA-seq) experiments. In this paper, we describe TopHat2, which incorporates many significant enhancements to TopHat. TopHat2 can align reads of various lengths produced by the latest sequencing technologies, while allowing for variable-length indels with respect to the reference genome. In addition to de novo spliced alignment, TopHat2 can align reads across fusion breaks, which can occur after genomic translocations. TopHat2 combines the ability to identify novel splice sites with direct mapping to known transcripts, producing sensitive and accurate alignments, even for highly repetitive genomes or in the presence of pseudogenes. TopHat2 is available at http://ccb.jhu.edu/software/tophat. More... »

PAGES

r36

Journal

TITLE

Genome Biology

ISSUE

4

VOLUME

14

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1186/gb-2013-14-4-r36

    DOI

    http://dx.doi.org/10.1186/gb-2013-14-4-r36

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1015459845

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/23618408


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