5 citations · 5 across the 1 of their papers we have counts for
2 papers
q-bio.GN2025★ 5 cited
Finding easy regions for short-read variant calling from pangenome data
Heng Li
Background: While benchmarks on short-read variant calling suggest low error rate below 0.5%, they are only applicable to predefined confident regions. For a human sample without s…
q-bio.GN2023
Scalable telomere-to-telomere assembly for diploid and polyploid genomes with double graph
Haoyu Cheng, Mobin Asri, Julian Lucas +2
Despite recent advances in the length and the accuracy of long-read data, building haplotype-resolved genome assemblies from telomere to telomere still requires considerable comput…