Đang chuẩn bị liên kết để tải về tài liệu:
HapCHAT: Adaptive haplotype assembly for efficiently leveraging high coverage in long reads

Haplotype assembly is the process of assigning the different alleles of the variants covered by mapped sequencing reads to the two haplotypes of the genome of a human individual. Long reads, which are nowadays cheaper to produce and more widely available than ever before, have been used to reduce the fragmentation of the assembled haplotypes since their ability to span several variants along the genome. |