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CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data
Single nucleotide polymorphisms (SNPs) are used widely for detecting quantitative trait loci, or for searching for causal variants of diseases. Nevertheless, structural variations such as copy-number variants (CNVs) represent a large part of natural genetic diversity, and contribute significantly to...
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| Publicado no: | Genetics |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Genetics Society of America
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7054022/ https://ncbi.nlm.nih.gov/pubmed/31882400 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/genetics.119.302881 |
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