TAP: a targeted clinical genomics pipeline for detecting transcript variants using RNA-seq data
Abstract Background RNA-seq is a powerful and cost-effective technology for molecular diagnostics of cancer and other diseases, and it can reach its full potential when coupled with validated clinical-grade informatics tools. Despite recent advances in long-read sequencing, transcriptome assembly of...
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Main Authors: | Readman Chiu (Author), Ka Ming Nip (Author), Justin Chu (Author), Inanc Birol (Author) |
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Format: | Book |
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BMC,
2018-09-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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