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Prioritizing disease-linked variants, genes, and pathways with an interactive whole genome analysis pipeline
Whole genome sequencing (WGS) studies are uncovering disease-associated variants in both rare and non-rare diseases. Utilizing the next-generation sequencing for WGS requires a series of computational methods for alignment, variant detection, and annotation, and the accuracy and reproducibility of a...
में बचाया:
| मुख्य लेखकों: | , , , , , , , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
2014
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4130156/ https://ncbi.nlm.nih.gov/pubmed/24478219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22520 |
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