Fig. 1.

The IGV screen capture of the selected variants. a A heterozygote SNP from T to G at chromosome 11, position 98,146,409 called only in the PacBio and ONT data, b a heterozygote deletion AA at chromosome 20, position 3,200,689 not called in all three technologies, c a heterozygote insertion ATCCTTCCT at chromosome 1, position 184,999,851 called only in the Illumina data, and d a heterozygote deletion G at chromosome 1, position 5,072,694 called in all three technologies. The tracks from top to down show the alignments of the Illumina, PacBio, and ONT reads from HG001 aligned to the human reference GRCh37