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PVAAS: identify variants associated with aberrant splicing from RNA-seq
Motivation: RNA-seq has been widely used to study the transcriptome. Comparing to microarray, sequencing-based RNA-seq is able to identify splicing variants and single nucleotide variants in one experiment simultaneously. This provides unique opportunity to detect variants that associated with aberr...
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| Опубликовано в: : | Bioinformatics |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Oxford University Press
2015
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4807355/ https://ncbi.nlm.nih.gov/pubmed/25573917 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv001 |
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