טוען...
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.
שמור ב:
| Main Authors: | , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2011
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| נושאים: | |
| גישה מקוונת: | 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 |
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