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Extracting allelic read counts from 250,000 human sequencing runs in Sequence Read Archive
The Sequence Read Archive (SRA) contains over one million publicly available sequencing runs from various studies using a variety of sequencing library strategies. These data inherently contain information about underlying genomic sequence variants which we exploit to extract allelic read counts on...
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| Publié dans: | Pac Symp Biocomput |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6415672/ https://ncbi.nlm.nih.gov/pubmed/30864322 |
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