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Haplotype Phasing and Inheritance of Copy Number Variants in Nuclear Families
DNA copy number variants (CNVs) that alter the copy number of a particular DNA segment in the genome play an important role in human phenotypic variability and disease susceptibility. A number of CNVs overlapping with genes have been shown to confer risk to a variety of human diseases thus highlight...
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| Veröffentlicht in: | PLoS One |
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| Hauptverfasser: | , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4390228/ https://ncbi.nlm.nih.gov/pubmed/25853576 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0122713 |
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