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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| 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 |