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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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| Publicat a: | BMC Genomics |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7686774/ https://ncbi.nlm.nih.gov/pubmed/33228531 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-020-07217-2 |
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