GCViT: a method for interactive, genome-wide visualization of resequencing and SNP array data

BACKGROUND: Large genotyping datasets have become commonplace due to efficient, cheap methods for SNP identification. Typical genotyping datasets may have thousands to millions of data points per accession, across tens to thousands of accessions. There is a need for tools to help rapidly explore suc...

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Detalles Bibliográficos
Autores principales: Wilkey, Andrew P., Brown, Anne V., Cannon, Steven B., Cannon, Ethalinda K. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686774/
https://www.ncbi.nlm.nih.gov/pubmed/33228531
http://dx.doi.org/10.1186/s12864-020-07217-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686774/
https://www.ncbi.nlm.nih.gov/pubmed/33228531
http://dx.doi.org/10.1186/s12864-020-07217-2

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