Abstract
A genomic sketch is a small, probabilistic representation of the set ofk-mers in a sequencing dataset. Sketches are building blocks for large-scale analyses that consider similarities between many pairs of sequences or sequence collections. While existing tools can easily compare 10,000s of genomes, relevant datasets can reach millions of sequences and beyond. Popular tools also fail to considerk-mer multiplicities, making them less applicable in quantitative settings. We describe a method called Dashing 2 that builds on the SetSketch data structure. SetSketch is related to HyperLogLog, but discards use of leading zero count in favor of a truncated logarithm of adjustable base. Unlike HLL, SetSketch can perform multiplicity-aware sketching when combined with the ProbMinHash method. Dashing 2 integrates locality-sensitive hashing to scale all-pairs comparisons to millions of sequences. Dashing 2 is free, open source software.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics (clinical),Genetics
Cited by
8 articles.
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