HandyCNV: Standardized Summary, Annotation, Comparison, and Visualization of Copy Number Variant, Copy Number Variation Region, and Runs of Homozygosity

Detection of CNVs (copy number variants) and ROH (runs of homozygosity) from SNP (single nucleotide polymorphism) genotyping data is often required in genomic studies. The post-analysis of CNV and ROH generally involves many steps, potentially across multiple computing platforms, which requires the...

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Detalles Bibliográficos
Autores principales: Zhou, Jinghang, Liu, Liyuan, Lopdell, Thomas J., Garrick, Dorian J., Shi, Yuangang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484803/
https://www.ncbi.nlm.nih.gov/pubmed/34603390
http://dx.doi.org/10.3389/fgene.2021.731355

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484803/
https://www.ncbi.nlm.nih.gov/pubmed/34603390
http://dx.doi.org/10.3389/fgene.2021.731355

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