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Estimating Genome-Wide Copy Number Using Allele-Specific Mixture Models
Genomic changes such as copy number alterations are one of the major underlying causes of human phenotypic variation among normal and disease subjects. Array comparative genomic hybridization (CGH) technology was developed to detect copy number changes in a high-throughput fashion. However, this tec...
Gorde:
| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Mary Ann Liebert, Inc.
2008
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2612042/ https://ncbi.nlm.nih.gov/pubmed/18707534 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/cmb.2007.0148 |
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