MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants
Abstract
The amount of genetic variation discovered in human populations is growing rapidly leading to challenging computational tasks, such as variant calling. Standard methods for addressing this problem include read mapping, a computationally expensive procedure; thus, mapping-free tools have been proposed in recent years. These tools focus on isolated, biallelic SNPs, providing limited support for multi-allelic SNPs and short insertions and deletions...
Paper Details
Title
MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants
Published Date
Aug 1, 2019
Journal
Volume
18
Pages
20 - 27
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