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Using XHMM software to detect copy number variation in whole-exome sequencing data
Copy number variation (CNV) has emerged as an important genetic component in human diseases, which are increasingly being studied for large numbers of samples by sequencing the coding regions of the genome, i.e., exome sequencing. Nonetheless, detecting this variation from such targeted sequencing d...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2014
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4065038/ https://ncbi.nlm.nih.gov/pubmed/24763994 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/0471142905.hg0723s81 |
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