paired end sequencing

This data resource is an outcome of the NSF RAPID project titled "Democratizing Genome Sequence Analysis for COVID-19 Using CloudLab" awarded to University of Missouri-Columbia.

The resource contains the output of variant analysis (along with CADD scores) on human genome sequences obtained from the COVID-19 Data Portal. The variants include single nucleotide polymorphisms (SNPs) and short insert and deletes (indels).