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CNV-guided multi-read allocation for ChIP-seq
Motivation: In chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) and other short-read sequencing experiments, a considerable fraction of the short reads align to multiple locations on the reference genome (multi-reads). Inferring the origin of multi-reads is critical fo...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4184254/ https://ncbi.nlm.nih.gov/pubmed/24966364 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu402 |
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