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Genotype calling and haplotyping in parent-offspring trios
Emerging sequencing technologies allow common and rare variants to be systematically assayed across the human genome in many individuals. In order to improve variant detection and genotype calling, raw sequence data are typically examined across many individuals. Here, we describe a method for genot...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3530674/ https://ncbi.nlm.nih.gov/pubmed/23064751 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.142455.112 |
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