Đang chuẩn bị liên kết để tải về tài liệu:
GeDi: Applying suffix arrays to increase the repertoire of detectable SNVs in tumour genomes

Current popular variant calling pipelines rely on the mapping coordinates of each input read to a reference genome in order to detect variants. Since reads deriving from variant loci that diverge in sequence substantially from the reference are often assigned incorrect mapping coordinates, variant calling pipelines that rely on mapping coordinates can exhibit reduced sensitivity. |