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SeeCiTe: a method to assess CNV calls from SNP arrays using trio data
MOTIVATION: Single nucleotide polymorphism (SNP) genotyping arrays remain an attractive platform for assaying copy number variants (CNVs) in large population-wide cohorts. However, current tools for calling CNVs are still prone to extensive false positive calls when applied to biobank scale arrays....
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8317106/ https://ncbi.nlm.nih.gov/pubmed/33459766 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btab028 |
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