posted on 2021-05-07, 17:39authored byLauren M. Lui, Torben N. Nielsen, Adam P. Arkin
Sequencing coverage graphs of genomes ERX2165959_bin_23, ERX2165959_bin_80, SRX1775573_bin_5, SRX1775577_bin_36, and SRX1775579_bin_0. Coverage is generally even with no areas of unusually low coverage. Variation in coverage at the ends of the chromosome are read-mapping artifacts since reads that span the chromosome ends may not map to these regions.