Automated genotyping of microsatellite loci from feces with high throughput sequences.

Ecological and conservation genetic studies often use noninvasive sampling, especially with elusive or endangered species. Because microsatellites are generally short in length, they can be amplified from low quality samples such as feces. Microsatellites are highly polymorphic so few markers are en...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Isabel Salado, Alberto Fernández-Gil, Carles Vilà, Jennifer A Leonard
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/72339b444d4f432eb7870439d2b30f63
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:72339b444d4f432eb7870439d2b30f63
record_format dspace
spelling oai:doaj.org-article:72339b444d4f432eb7870439d2b30f632021-12-02T20:13:32ZAutomated genotyping of microsatellite loci from feces with high throughput sequences.1932-620310.1371/journal.pone.0258906https://doaj.org/article/72339b444d4f432eb7870439d2b30f632021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0258906https://doaj.org/toc/1932-6203Ecological and conservation genetic studies often use noninvasive sampling, especially with elusive or endangered species. Because microsatellites are generally short in length, they can be amplified from low quality samples such as feces. Microsatellites are highly polymorphic so few markers are enough for reliable individual identification, kinship determination, or population characterization. However, the genotyping process from feces is expensive and time consuming. Given next-generation sequencing (NGS) and recent software developments, automated microsatellite genotyping from NGS data may now be possible. These software packages infer the genotypes directly from sequence reads, increasing throughput. Here we evaluate the performance of four software packages to genotype microsatellite loci from Iberian wolf (Canis lupus) feces using NGS. We initially combined 46 markers in a single multiplex reaction for the first time, of which 19 were included in the final analyses. Megasat was the software that provided genotypes with fewer errors. Coverage over 100X provided little additional information, but a relatively high number of PCR replicates were necessary to obtain a high quality genotype from highly unoptimized, multiplexed reactions (10 replicates for 18 of the 19 loci analyzed here). This could be reduced through optimization. The use of new bioinformatic tools and next-generation sequencing data to genotype these highly informative markers may increase throughput at a reasonable cost and with a smaller amount of laboratory work. Thus, high throughput sequencing approaches could facilitate the use of microsatellites with fecal DNA to address ecological and conservation questions.Isabel SaladoAlberto Fernández-GilCarles VilàJennifer A LeonardPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 10, p e0258906 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Isabel Salado
Alberto Fernández-Gil
Carles Vilà
Jennifer A Leonard
Automated genotyping of microsatellite loci from feces with high throughput sequences.
description Ecological and conservation genetic studies often use noninvasive sampling, especially with elusive or endangered species. Because microsatellites are generally short in length, they can be amplified from low quality samples such as feces. Microsatellites are highly polymorphic so few markers are enough for reliable individual identification, kinship determination, or population characterization. However, the genotyping process from feces is expensive and time consuming. Given next-generation sequencing (NGS) and recent software developments, automated microsatellite genotyping from NGS data may now be possible. These software packages infer the genotypes directly from sequence reads, increasing throughput. Here we evaluate the performance of four software packages to genotype microsatellite loci from Iberian wolf (Canis lupus) feces using NGS. We initially combined 46 markers in a single multiplex reaction for the first time, of which 19 were included in the final analyses. Megasat was the software that provided genotypes with fewer errors. Coverage over 100X provided little additional information, but a relatively high number of PCR replicates were necessary to obtain a high quality genotype from highly unoptimized, multiplexed reactions (10 replicates for 18 of the 19 loci analyzed here). This could be reduced through optimization. The use of new bioinformatic tools and next-generation sequencing data to genotype these highly informative markers may increase throughput at a reasonable cost and with a smaller amount of laboratory work. Thus, high throughput sequencing approaches could facilitate the use of microsatellites with fecal DNA to address ecological and conservation questions.
format article
author Isabel Salado
Alberto Fernández-Gil
Carles Vilà
Jennifer A Leonard
author_facet Isabel Salado
Alberto Fernández-Gil
Carles Vilà
Jennifer A Leonard
author_sort Isabel Salado
title Automated genotyping of microsatellite loci from feces with high throughput sequences.
title_short Automated genotyping of microsatellite loci from feces with high throughput sequences.
title_full Automated genotyping of microsatellite loci from feces with high throughput sequences.
title_fullStr Automated genotyping of microsatellite loci from feces with high throughput sequences.
title_full_unstemmed Automated genotyping of microsatellite loci from feces with high throughput sequences.
title_sort automated genotyping of microsatellite loci from feces with high throughput sequences.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/72339b444d4f432eb7870439d2b30f63
work_keys_str_mv AT isabelsalado automatedgenotypingofmicrosatellitelocifromfeceswithhighthroughputsequences
AT albertofernandezgil automatedgenotypingofmicrosatellitelocifromfeceswithhighthroughputsequences
AT carlesvila automatedgenotypingofmicrosatellitelocifromfeceswithhighthroughputsequences
AT jenniferaleonard automatedgenotypingofmicrosatellitelocifromfeceswithhighthroughputsequences
_version_ 1718374772203585536