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Insertion-deletion polymorphisms (indels) as genetic markers in natural populations
BACKGROUND: We introduce the use of short insertion-deletion polymorphisms (indels) for genetic analysis of natural populations. RESULTS: Sequence reads from light shot-gun sequencing efforts of different dog breeds were aligned to the dog genome reference sequence and gaps corresponding to indels w...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266919/ https://www.ncbi.nlm.nih.gov/pubmed/18211670 http://dx.doi.org/10.1186/1471-2156-9-8 |
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author | Väli, Ülo Brandström, Mikael Johansson, Malin Ellegren, Hans |
author_facet | Väli, Ülo Brandström, Mikael Johansson, Malin Ellegren, Hans |
author_sort | Väli, Ülo |
collection | PubMed |
description | BACKGROUND: We introduce the use of short insertion-deletion polymorphisms (indels) for genetic analysis of natural populations. RESULTS: Sequence reads from light shot-gun sequencing efforts of different dog breeds were aligned to the dog genome reference sequence and gaps corresponding to indels were identified. One hundred candidate markers (4-bp indels) were selected and genotyped in unrelated dogs (n = 7) and wolves (n = 18). Eighty-one and 76 out of 94 could be validated as polymorphic loci in the respective sample. Mean indel heterozygosity in a diverse set of wolves was 19%, and 74% of the loci had a minor allele frequency of >10%. Indels found to be polymorphic in wolves were subsequently genotyped in a highly bottlenecked Scandinavian wolf population. Fifty-one loci turned out to be polymorphic, showing their utility even in a population with low genetic diversity. In this population, individual heterozygosity measured at indel and microsatellite loci were highly correlated. CONCLUSION: With an increasing amount of sequence information gathered from non-model organisms, we suggest that indels will come to form an important source of genetic markers, easy and cheap to genotype, for studies of natural populations. |
format | Text |
id | pubmed-2266919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22669192008-03-12 Insertion-deletion polymorphisms (indels) as genetic markers in natural populations Väli, Ülo Brandström, Mikael Johansson, Malin Ellegren, Hans BMC Genet Research Article BACKGROUND: We introduce the use of short insertion-deletion polymorphisms (indels) for genetic analysis of natural populations. RESULTS: Sequence reads from light shot-gun sequencing efforts of different dog breeds were aligned to the dog genome reference sequence and gaps corresponding to indels were identified. One hundred candidate markers (4-bp indels) were selected and genotyped in unrelated dogs (n = 7) and wolves (n = 18). Eighty-one and 76 out of 94 could be validated as polymorphic loci in the respective sample. Mean indel heterozygosity in a diverse set of wolves was 19%, and 74% of the loci had a minor allele frequency of >10%. Indels found to be polymorphic in wolves were subsequently genotyped in a highly bottlenecked Scandinavian wolf population. Fifty-one loci turned out to be polymorphic, showing their utility even in a population with low genetic diversity. In this population, individual heterozygosity measured at indel and microsatellite loci were highly correlated. CONCLUSION: With an increasing amount of sequence information gathered from non-model organisms, we suggest that indels will come to form an important source of genetic markers, easy and cheap to genotype, for studies of natural populations. BioMed Central 2008-01-22 /pmc/articles/PMC2266919/ /pubmed/18211670 http://dx.doi.org/10.1186/1471-2156-9-8 Text en Copyright © 2008 Väli et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Väli, Ülo Brandström, Mikael Johansson, Malin Ellegren, Hans Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title | Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title_full | Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title_fullStr | Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title_full_unstemmed | Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title_short | Insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
title_sort | insertion-deletion polymorphisms (indels) as genetic markers in natural populations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266919/ https://www.ncbi.nlm.nih.gov/pubmed/18211670 http://dx.doi.org/10.1186/1471-2156-9-8 |
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