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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...
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| Main Authors: | , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3218660/ https://ncbi.nlm.nih.gov/pubmed/20964841 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2010-11-10-r104 |
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