FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing data
We have developed FusionSeq to identify fusion transcripts from paired-end RNA-sequencing. FusionSeq includes filters to remove spurious candidate fusions with artifacts, such as misalignment or random pairing of transcript fragments, and it ranks candidates according to several statistics. It also...
Main Authors: | Sboner, Andrea, Habegger, Lukas, Pflueger, Dorothee, Terry, Stephane, Chen, David Z, Rozowsky, Joel S, Tewari, Ashutosh K, Kitabayashi, Naoki, Moss, Benjamin J, Chee, Mark S, Demichelis, Francesca, Rubin, Mark A, Gerstein, Mark B |
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Format: | Online |
Language: | English |
Published: |
BioMed Central
2010
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218660/ |
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