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Reducing the search space for causal genetic variants with VASP
Motivation: Increasingly, cost-effective high-throughput DNA sequencing technologies are being utilized to sequence human pedigrees to elucidate the genetic cause of a wide variety of human diseases. While numerous tools exist for variant prioritization within a single genome, the ability to concurr...
में बचाया:
| में प्रकाशित: | Bioinformatics |
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| मुख्य लेखकों: | , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Oxford University Press
2015
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4495293/ https://ncbi.nlm.nih.gov/pubmed/25755272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv135 |
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