Multiplexing with three-primer PCR for rapid and economical microsatellite validation.

The next generation sequencing revolution has enabled rapid discovery of genetic markers, however, development of fully functioning new markers still requires a long and costly process of marker validation. This study reports a rapid and economical approach for the validation and deployment of polym...

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Published in:Hereditas
Main Authors: Vartia, Salla, Collins, Patrick C., Cross, Thomas F., Fitzgerald, Richard D., Gauthier, David T., McGinnity, Philip, Mirimin, Luca, Carlsson, Jens
Format: Article in Journal/Newspaper
Language:English
Published: 2014
Subjects:
Online Access:https://pure.qub.ac.uk/en/publications/multiplexing-with-threeprimer-pcr-for-rapid-and-economical-microsatellite-validation(0e0d2f2a-4a5a-40da-b6a0-842ec7560594).html
https://doi.org/10.1111/hrd2.00044
https://pureadmin.qub.ac.uk/ws/files/17942257/epdf.mht
id ftqueensubelpubl:oai:pure.qub.ac.uk/portal:publications/0e0d2f2a-4a5a-40da-b6a0-842ec7560594
record_format openpolar
spelling ftqueensubelpubl:oai:pure.qub.ac.uk/portal:publications/0e0d2f2a-4a5a-40da-b6a0-842ec7560594 2023-05-15T15:27:35+02:00 Multiplexing with three-primer PCR for rapid and economical microsatellite validation. Vartia, Salla Collins, Patrick C. Cross, Thomas F. Fitzgerald, Richard D. Gauthier, David T. McGinnity, Philip Mirimin, Luca Carlsson, Jens 2014-06 message/rfc822 https://pure.qub.ac.uk/en/publications/multiplexing-with-threeprimer-pcr-for-rapid-and-economical-microsatellite-validation(0e0d2f2a-4a5a-40da-b6a0-842ec7560594).html https://doi.org/10.1111/hrd2.00044 https://pureadmin.qub.ac.uk/ws/files/17942257/epdf.mht eng eng info:eu-repo/semantics/openAccess Vartia , S , Collins , P C , Cross , T F , Fitzgerald , R D , Gauthier , D T , McGinnity , P , Mirimin , L & Carlsson , J 2014 , ' Multiplexing with three-primer PCR for rapid and economical microsatellite validation. ' , Hereditas , vol. 151 , no. 2-3 , pp. 43-54 . https://doi.org/10.1111/hrd2.00044 Next generation sequencing article 2014 ftqueensubelpubl https://doi.org/10.1111/hrd2.00044 2022-02-09T22:18:59Z The next generation sequencing revolution has enabled rapid discovery of genetic markers, however, development of fully functioning new markers still requires a long and costly process of marker validation. This study reports a rapid and economical approach for the validation and deployment of polymorphic microsatellite markers obtained from a 454 pyrosequencing library of Atlantic cod, Gadus morhua, Linnaeus 1758. Primers were designed from raw reads to amplify specific amplicon size ranges, allowing effective PCR multiplexing. Multiplexing was combined with a three-primer PCR approach using four universal tails to label amplicons with separate fluorochromes. A total of 192 primer pairs were tested, resulting in 73 polymorphic markers. Of these, 55 loci were combined in six multiplex panels each containing between six and eleven markers. Variability of the loci was assessed on G. morhua from the Celtic Sea (n 46) and the Scotian Shelf (n 46), two locations that have shown genetic differentiation in previous studies. Multilocus FST between the two samples was estimated at 0.067 (P 0.001). After three loci potentially under selection were excluded, the global FST was estimated at 0.043 (P 0.001). Our technique combines three- primer and multiplex PCR techniques, allowing simultaneous screening and validation of relatively large numbers of microsatellite loci. Article in Journal/Newspaper atlantic cod Gadus morhua Queen's University Belfast Research Portal Hereditas 151 2-3 43 54
institution Open Polar
collection Queen's University Belfast Research Portal
op_collection_id ftqueensubelpubl
language English
topic Next generation sequencing
spellingShingle Next generation sequencing
Vartia, Salla
Collins, Patrick C.
Cross, Thomas F.
Fitzgerald, Richard D.
Gauthier, David T.
McGinnity, Philip
Mirimin, Luca
Carlsson, Jens
Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
topic_facet Next generation sequencing
description The next generation sequencing revolution has enabled rapid discovery of genetic markers, however, development of fully functioning new markers still requires a long and costly process of marker validation. This study reports a rapid and economical approach for the validation and deployment of polymorphic microsatellite markers obtained from a 454 pyrosequencing library of Atlantic cod, Gadus morhua, Linnaeus 1758. Primers were designed from raw reads to amplify specific amplicon size ranges, allowing effective PCR multiplexing. Multiplexing was combined with a three-primer PCR approach using four universal tails to label amplicons with separate fluorochromes. A total of 192 primer pairs were tested, resulting in 73 polymorphic markers. Of these, 55 loci were combined in six multiplex panels each containing between six and eleven markers. Variability of the loci was assessed on G. morhua from the Celtic Sea (n 46) and the Scotian Shelf (n 46), two locations that have shown genetic differentiation in previous studies. Multilocus FST between the two samples was estimated at 0.067 (P 0.001). After three loci potentially under selection were excluded, the global FST was estimated at 0.043 (P 0.001). Our technique combines three- primer and multiplex PCR techniques, allowing simultaneous screening and validation of relatively large numbers of microsatellite loci.
format Article in Journal/Newspaper
author Vartia, Salla
Collins, Patrick C.
Cross, Thomas F.
Fitzgerald, Richard D.
Gauthier, David T.
McGinnity, Philip
Mirimin, Luca
Carlsson, Jens
author_facet Vartia, Salla
Collins, Patrick C.
Cross, Thomas F.
Fitzgerald, Richard D.
Gauthier, David T.
McGinnity, Philip
Mirimin, Luca
Carlsson, Jens
author_sort Vartia, Salla
title Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
title_short Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
title_full Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
title_fullStr Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
title_full_unstemmed Multiplexing with three-primer PCR for rapid and economical microsatellite validation.
title_sort multiplexing with three-primer pcr for rapid and economical microsatellite validation.
publishDate 2014
url https://pure.qub.ac.uk/en/publications/multiplexing-with-threeprimer-pcr-for-rapid-and-economical-microsatellite-validation(0e0d2f2a-4a5a-40da-b6a0-842ec7560594).html
https://doi.org/10.1111/hrd2.00044
https://pureadmin.qub.ac.uk/ws/files/17942257/epdf.mht
genre atlantic cod
Gadus morhua
genre_facet atlantic cod
Gadus morhua
op_source Vartia , S , Collins , P C , Cross , T F , Fitzgerald , R D , Gauthier , D T , McGinnity , P , Mirimin , L & Carlsson , J 2014 , ' Multiplexing with three-primer PCR for rapid and economical microsatellite validation. ' , Hereditas , vol. 151 , no. 2-3 , pp. 43-54 . https://doi.org/10.1111/hrd2.00044
op_rights info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.1111/hrd2.00044
container_title Hereditas
container_volume 151
container_issue 2-3
container_start_page 43
op_container_end_page 54
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