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Computational and statistical approaches to analyzing variants identified by exome sequencing
New sequencing technology has enabled the identification of thousands of single nucleotide polymorphisms in the exome, and many computational and statistical approaches to identify disease-association signals have emerged.
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
BioMed Central
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3308043/ https://ncbi.nlm.nih.gov/pubmed/21920052 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2011-12-9-227 |
| Etiketak: |
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