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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...
में बचाया:
| में प्रकाशित: | BMC Genomics |
|---|---|
| मुख्य लेखकों: | , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BioMed Central
2020
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| विषय: | |
| ऑनलाइन पहुंच: | 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 |
| टैग : |
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