טוען...
Variant detection sensitivity and biases in whole genome and exome sequencing
BACKGROUND: Less than two percent of the human genome is protein coding, yet that small fraction harbours the majority of known disease causing mutations. Despite rapidly falling whole genome sequencing (WGS) costs, much research and increasingly the clinical use of sequence data is likely to remain...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4122774/ https://ncbi.nlm.nih.gov/pubmed/25038816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-15-247 |
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