2022
DOI: 10.1101/2022.10.27.514110
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Demographically explicit scans for barriers to gene flow using gIMble

Abstract: Identifying regions of the genome that act as barriers to gene flow between recently diverged taxa has remained challenging given the many evolutionary forces that generate variation in genetic diversity and divergence along the genome and the stochastic nature of this variation. Here we implement a composite likelihood approach for quantifying barriers to gene flow. This analytic framework captures background selection and selection against maladaptive alleles, i.e. genomic barriers, in a model of isolation w… Show more

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Cited by 17 publications
(62 citation statements)
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“…We use gIMble (Laetsch et al 2022), a recent implementation of a blockwise likelihood calculation (Lohse et al 2016), to infer the demographic history of speciation between B. daphne and B.…”
Section: Demographic Historymentioning
confidence: 99%
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“…We use gIMble (Laetsch et al 2022), a recent implementation of a blockwise likelihood calculation (Lohse et al 2016), to infer the demographic history of speciation between B. daphne and B.…”
Section: Demographic Historymentioning
confidence: 99%
“…Variant calls were filtered using gIMble preprocess (Laetsch et al 2022), with the following options: --snpgap 2 --min qual 10 --min depth 8 --max depth 3, where --max depth is in units of mean coverage.…”
Section: Variant Calling and Filteringmentioning
confidence: 99%
See 1 more Smart Citation
“…We analysed mean genetic divergence (d XY ) and fitted models of species’ divergence with and without long-term interspecific gene flow between and within species using gIMble (Laetsch et al 2022). This analytic likelihood method uses the joint distribution of mutation types in short sequence blocks, the blockwise site frequency spectrum (bSFS) across subsamples of pairs of individual genomes to fit a series of models of speciation history.…”
Section: Methodsmentioning
confidence: 99%
“…The resulting BAM-files were used for variant calling with freebayes v1.3.1-dirty (Garrison and Marth 2012). Raw variants were processed with gIMble preprocess (genome-wide IM blockwise likelihood estimation toolkit; (Laetsch et al 2022)). In brief, non-SNP variants were deconstructed into allelic primitives, where remaining non-SNPs were removed in addition to any SNP variant within two bp of a non-SNP.…”
Section: Mapping Variant Calling and Variant Filteringmentioning
confidence: 99%