Article
GCViT: a method for interactive, genome-wide visualization of resequencing and SNP array data.
BMC genomics - 23 Nov 2020
Wilkey Andrew P, Brown Anne V, Cannon Steven B, Cannon Ethalinda K S
Abstract excerpt
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 such datasets, to assess characteristics such as overall differences between accessions and regional anomalies across...
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