selscan: An Efficient Multithreaded Program to Perform EHH-Based Scans for Positive Selection
Year: 2014
Type: article
Abstract: Haplotype-based scans to detect natural selection are useful to identify recent or ongoing positive selection in genomes. As both real and simulated genomic data sets grow larger, spanning thousands of samples and millions of markers, there is a need for a fast and efficient implementation of these scans for general use. Here, we present selscan, an efficient multithreaded application that implements Extended Haplotype Homozygosity (EHH), Integrated Haplotype Score (iHS), and Cross-population EHH (XPEHH). selscan accepts phased genotypes in multiple formats, including TPED, and performs extremely well on both simulated and real data and over an order of magnitude faster than existing available implementations. It calculates iHS on chromosome 22 (22,147 loci) across 204 CEU haplotypes in 353 s on one thread (33 s on 16 threads) and calculates XPEHH for the same data relative to 210 YRI haplotypes in 578 s on one thread (52 s on 16 threads). Source code and binaries (Windows, OSX, and Linux) are available at https://github.com/szpiech/selscan.
Source: Molecular Biology and Evolution
Authors: Z. A. Szpiech, R. D. Hernandez
Institutions: University of California, San Francisco, QB3
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $3,418
Funders: Alfred P. Sloan Foundation, National Institutes of Health, National Heart, Lung, and Blood Institute, National Human Genome Research Institute, National Cancer Institute, National Center for Research Resources, National Center for Advancing Translational Sciences, National Institute on Minority Health and Health Disparities
Awards: Clinical and Translational Science Institute, G2189466114, Addressing disparities in chronic disease with a teen and young adult focus, G36189942, G3637141366, G483408255, G7396086925, Retention of somatic mutations in cancers by changes in pH sensing, Accurate, long-read sequencing with droplet-microfluidic barcoding, G7884706843, G8272085470, G9000096963, G9000330731
OpenAlex ID: W2133298050
