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A new method for ecologists to estimate heterozygote excess and deficit for multi‐locus gene families
The fixation index, FIS, has been a staple measure to detect selection, or departures from random mating in populations. However, current Next Generation Sequencing (NGS) cannot easily estimate FIS, in multi‐locus gene families that contain multiple loci having similar or identical arrays of variant...
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description | The fixation index, FIS, has been a staple measure to detect selection, or departures from random mating in populations. However, current Next Generation Sequencing (NGS) cannot easily estimate FIS, in multi‐locus gene families that contain multiple loci having similar or identical arrays of variant sequences of ≥1 kilobase (kb), which differ at multiple positions. In these families, high‐quality short‐read NGS data typically identify variants, but not the genomic location, which is required to calculate FIS (based on locus‐specific observed and expected heterozygosity). Thus, to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, we need a method that does not require knowledge of which variants are alleles at which locus in the genome. We developed such a method. Like FIS, our novel measure, 1HIS, is based on the principle that positive assortative mating, or selection against heterozygotes, and some other processes reduce within‐individual variability relative to the population. We demonstrate high accuracy of 1HIS on a wide range of simulated scenarios and two datasets from natural populations of penguins and dolphins. 1HIS is important because multi‐locus gene families are often involved in assortative mating or selection on heterozygotes. 1HIS is particularly useful for multi‐locus gene families, such as toll‐like receptors, the major histocompatibility complex in animals, homeobox genes in fungi and self‐incompatibility genes in plants.
The fixation index, FIS, has been a staple measure to assess assortative mating or selection on heterozygotes. However, current Next Generation Sequencing (NGS) cannot easily determine which variants are allelic at which locus—a requirement to calculate FIS. We have developed a method called H1IS$$ {{}^1H}_{IS} $$ to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, that does not require knowledge of which variants are allelic at which locus in the genome. |
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The fixation index, FIS, has been a staple measure to assess assortative mating or selection on heterozygotes. However, current Next Generation Sequencing (NGS) cannot easily determine which variants are allelic at which locus—a requirement to calculate FIS. We have developed a method called H1IS$$ {{}^1H}_{IS} $$ to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, that does not require knowledge of which variants are allelic at which locus in the genome.</description><identifier>ISSN: 2045-7758</identifier><identifier>EISSN: 2045-7758</identifier><identifier>DOI: 10.1002/ece3.11561</identifier><identifier>PMID: 39045501</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Animal reproduction ; Assortative mating ; Conservation Genetics ; Ecological Genetics ; Equilibrium ; Evolutionary Ecology ; F IS ; fixation index ; Gene families ; Gene sequencing ; Genes ; Genetics ; Genomes ; Heterozygotes ; Homeobox ; inbreeding ; Incompatibility ; Major histocompatibility complex ; Mating ; Natural populations ; Next-generation sequencing ; Polymorphism ; Population ; Population Genetics ; Populations ; selection ; Self-incompatibility ; simulation ; Toll-like receptors</subject><ispartof>Ecology and evolution, 2024-07, Vol.14 (7), p.e11561-n/a</ispartof><rights>2024 The Author(s). published by John Wiley & Sons Ltd.</rights><rights>2024 The Author(s). Ecology and Evolution published by John Wiley & Sons Ltd.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4431-143efb8aa09eb4ea46aaeb54fd81a9bbb07c7a78c0a147ac1cd96a7cc399281e3</cites><orcidid>0000-0002-8527-5593 ; 0000-0002-0924-3768 ; 0000-0002-1578-8473</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3086249877/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3086249877?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11561,25752,27923,27924,37011,37012,44589,46051,46475,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39045501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Reilly, Gabe D.</creatorcontrib><creatorcontrib>Manlik, Oliver</creatorcontrib><creatorcontrib>Vardeh, Sandra</creatorcontrib><creatorcontrib>Sinclair, Jennifer</creatorcontrib><creatorcontrib>Cannell, Belinda</creatorcontrib><creatorcontrib>Lawler, Zachary P.</creatorcontrib><creatorcontrib>Sherwin, William B.</creatorcontrib><title>A new method for ecologists to estimate heterozygote excess and deficit for multi‐locus gene families</title><title>Ecology and evolution</title><addtitle>Ecol Evol</addtitle><description>The fixation index, FIS, has been a staple measure to detect selection, or departures from random mating in populations. However, current Next Generation Sequencing (NGS) cannot easily estimate FIS, in multi‐locus gene families that contain multiple loci having similar or identical arrays of variant sequences of ≥1 kilobase (kb), which differ at multiple positions. In these families, high‐quality short‐read NGS data typically identify variants, but not the genomic location, which is required to calculate FIS (based on locus‐specific observed and expected heterozygosity). Thus, to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, we need a method that does not require knowledge of which variants are alleles at which locus in the genome. We developed such a method. Like FIS, our novel measure, 1HIS, is based on the principle that positive assortative mating, or selection against heterozygotes, and some other processes reduce within‐individual variability relative to the population. We demonstrate high accuracy of 1HIS on a wide range of simulated scenarios and two datasets from natural populations of penguins and dolphins. 1HIS is important because multi‐locus gene families are often involved in assortative mating or selection on heterozygotes. 1HIS is particularly useful for multi‐locus gene families, such as toll‐like receptors, the major histocompatibility complex in animals, homeobox genes in fungi and self‐incompatibility genes in plants.
The fixation index, FIS, has been a staple measure to assess assortative mating or selection on heterozygotes. However, current Next Generation Sequencing (NGS) cannot easily determine which variants are allelic at which locus—a requirement to calculate FIS. 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However, current Next Generation Sequencing (NGS) cannot easily estimate FIS, in multi‐locus gene families that contain multiple loci having similar or identical arrays of variant sequences of ≥1 kilobase (kb), which differ at multiple positions. In these families, high‐quality short‐read NGS data typically identify variants, but not the genomic location, which is required to calculate FIS (based on locus‐specific observed and expected heterozygosity). Thus, to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, we need a method that does not require knowledge of which variants are alleles at which locus in the genome. We developed such a method. Like FIS, our novel measure, 1HIS, is based on the principle that positive assortative mating, or selection against heterozygotes, and some other processes reduce within‐individual variability relative to the population. We demonstrate high accuracy of 1HIS on a wide range of simulated scenarios and two datasets from natural populations of penguins and dolphins. 1HIS is important because multi‐locus gene families are often involved in assortative mating or selection on heterozygotes. 1HIS is particularly useful for multi‐locus gene families, such as toll‐like receptors, the major histocompatibility complex in animals, homeobox genes in fungi and self‐incompatibility genes in plants.
The fixation index, FIS, has been a staple measure to assess assortative mating or selection on heterozygotes. However, current Next Generation Sequencing (NGS) cannot easily determine which variants are allelic at which locus—a requirement to calculate FIS. We have developed a method called H1IS$$ {{}^1H}_{IS} $$ to assess assortative mating, or selection on heterozygotes, from NGS of multi‐locus gene families, that does not require knowledge of which variants are allelic at which locus in the genome.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>39045501</pmid><doi>10.1002/ece3.11561</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-8527-5593</orcidid><orcidid>https://orcid.org/0000-0002-0924-3768</orcidid><orcidid>https://orcid.org/0000-0002-1578-8473</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal reproduction Assortative mating Conservation Genetics Ecological Genetics Equilibrium Evolutionary Ecology F IS fixation index Gene families Gene sequencing Genes Genetics Genomes Heterozygotes Homeobox inbreeding Incompatibility Major histocompatibility complex Mating Natural populations Next-generation sequencing Polymorphism Population Population Genetics Populations selection Self-incompatibility simulation Toll-like receptors |
title | A new method for ecologists to estimate heterozygote excess and deficit for multi‐locus gene families |
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