Fig. 6From: NanoCaller for accurate detection of SNPs and indels in difficult-to-map regions from long-read sequencing by haplotype-aware deep neural networksEvidence for novel deletions. a IGV plots of Nanopore, PacBio CCS, and Illumina reads of HG002 genome at chr9:135663780-135663850. The 40-bp-long deletion shown below in black box was identified using Sanger sequencing at chr9:135663795 or chr9:135663804 (both are correct and the difference is due to two different alignments). b Sanger sequencing signal data around the deletionBack to article page