Fast genotyping of known SNPs through approximate
Author(s)Shajii, Ariya; Yorukoglu, Deniz; Yu, Yun William; Berger Leighton, Bonnie
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Motivation: As the volume of next-generation sequencing (NGS) data increases, faster algorithms become necessary. Although speeding up individual components of a sequence analysis pipeline (e.g. read mapping) can reduce the computational cost of analysis, such approaches do not take full advantage of the particulars of a given problem. One problem of great interest, genotyping a known set of variants (e.g. dbSNP or Affymetrix SNPs), is important for characterization of known genetic traits and causative disease variants within an individual, as well as the initial stage of many ancestral and population genomic pipelines (e.g. GWAS). Results: We introduce lightweight assignment of variant alleles (LAVA), an NGS-based genotyping algorithm for a given set of SNP loci, which takes advantage of the fact that approximate matching of mid-size k-mers (with k = 32) can typically uniquely ide ntify loci in the human genome without full read alignment. LAVA accurately calls the vast majority of SNPs in dbSNP and Affymetrix's Genome-Wide Human SNP Array 6.0 up to about an order of magnitude faster than standard NGS genotyping pipelines. For Affymetrix SNPs, LAVA has significantly higher SNP calling accuracy than existing pipelines while using as low as ∼5 GB of RAM. As such, LAVA represents a scalable computational method for population-level genotyping studies as well as a flexible NGS-based replacement for SNP arrays. Availability and Implementation: LAVA software is available at http://lava.csail.mit.edu.
DepartmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory; Massachusetts Institute of Technology. Department of Mathematics
Oxford University Press (OUP)
Shajii, Ariya et al. “Fast Genotyping of Known SNPs through Approximatek-Mer Matching.” Bioinformatics 32, 17 (September 2016): i538–i544 © 2016 The Authors
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