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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2014
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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 |
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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 |
_version_ |
1766358012134424576 |