read_haps: using read haplotypes to detect same species contamination in DNA sequences.
Where this comes from
- Record sourced from PubMed, PMID 33135043.
- Also identified by DOI 10.1093/bioinformatics/btaa936.
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Abstract
Data analysis is requisite on reliable data. In genetics this includes verifying that the sample is not contaminated with another, a problem ubiquitous in biology. In human, and other diploid species, DNA contamination from the same species can be found by the presence of three haplotypes between polymorphic SNPs. read_haps is a tool that detects sample contamination from short read whole genome sequencing data. github.com/DecodeGenetics/read_haps.
Medical subject headings
- Diploidy
- High-Throughput Nucleotide Sequencing