A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.

A multistage testing strategy to detect QTL for resistance to infectious salmon anemia (ISA) in Atlantic salmon is proposed. First, genotyping of amplified fragment length polymorphisms (AFLP) and a transmission disequilibrium test (TDT) were carried out using dead offspring from a disease resistanc...

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Published in:Genetics
Main Authors: Moen, Thomas, Fjalestad, Kjersti T, Munck, Hege, Gomez-Raya, Luis
Format: Text
Language:English
Published: 2004
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1470919
http://www.ncbi.nlm.nih.gov/pubmed/15238533
https://doi.org/10.1534/genetics.103.013227
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spelling ftpubmed:oai:pubmedcentral.nih.gov:1470919 2023-05-15T15:30:46+02:00 A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon. Moen, Thomas Fjalestad, Kjersti T Munck, Hege Gomez-Raya, Luis 2004-06 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1470919 http://www.ncbi.nlm.nih.gov/pubmed/15238533 https://doi.org/10.1534/genetics.103.013227 en eng http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1470919 http://www.ncbi.nlm.nih.gov/pubmed/15238533 http://dx.doi.org/10.1534/genetics.103.013227 Research Article Text 2004 ftpubmed https://doi.org/10.1534/genetics.103.013227 2013-08-31T01:58:27Z A multistage testing strategy to detect QTL for resistance to infectious salmon anemia (ISA) in Atlantic salmon is proposed. First, genotyping of amplified fragment length polymorphisms (AFLP) and a transmission disequilibrium test (TDT) were carried out using dead offspring from a disease resistance challenge test. Second, AFLP genotyping among survivors followed by a Mendelian segregation test was performed. Third, within-family survival analyses using all offspring were developed and applied to significant TDT markers with Mendelian inheritance. Maximum-likelihood methodology was developed for TDT with dominant markers to exploit linkage disequilibrium within families. The strategy was tested with two full-sib families of Atlantic salmon sired by the same male and consisting of 79 offspring in total. All dead offspring from the two families were typed for 64 primer combinations, resulting in 340 scored markers. There were 26 significant results out of 401 TDTs using dead offspring. In the second stage, only 17 marker families showed Mendelian segregation and were tested in survival analysis. A permutation test was performed for all survival analyses to compute experimentwise P-values. Two markers, aaccac356 and agccta150, were significant at P < 0.05 when accounting for multiple testing in the survival analyses. The proposed strategy might be more powerful than current mapping strategies because it reduces the number of tests to be performed in the last testing stage. Text Atlantic salmon PubMed Central (PMC) Genetics 167 2 851 858
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Moen, Thomas
Fjalestad, Kjersti T
Munck, Hege
Gomez-Raya, Luis
A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
topic_facet Research Article
description A multistage testing strategy to detect QTL for resistance to infectious salmon anemia (ISA) in Atlantic salmon is proposed. First, genotyping of amplified fragment length polymorphisms (AFLP) and a transmission disequilibrium test (TDT) were carried out using dead offspring from a disease resistance challenge test. Second, AFLP genotyping among survivors followed by a Mendelian segregation test was performed. Third, within-family survival analyses using all offspring were developed and applied to significant TDT markers with Mendelian inheritance. Maximum-likelihood methodology was developed for TDT with dominant markers to exploit linkage disequilibrium within families. The strategy was tested with two full-sib families of Atlantic salmon sired by the same male and consisting of 79 offspring in total. All dead offspring from the two families were typed for 64 primer combinations, resulting in 340 scored markers. There were 26 significant results out of 401 TDTs using dead offspring. In the second stage, only 17 marker families showed Mendelian segregation and were tested in survival analysis. A permutation test was performed for all survival analyses to compute experimentwise P-values. Two markers, aaccac356 and agccta150, were significant at P < 0.05 when accounting for multiple testing in the survival analyses. The proposed strategy might be more powerful than current mapping strategies because it reduces the number of tests to be performed in the last testing stage.
format Text
author Moen, Thomas
Fjalestad, Kjersti T
Munck, Hege
Gomez-Raya, Luis
author_facet Moen, Thomas
Fjalestad, Kjersti T
Munck, Hege
Gomez-Raya, Luis
author_sort Moen, Thomas
title A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
title_short A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
title_full A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
title_fullStr A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
title_full_unstemmed A multistage testing strategy for detection of quantitative trait Loci affecting disease resistance in Atlantic salmon.
title_sort multistage testing strategy for detection of quantitative trait loci affecting disease resistance in atlantic salmon.
publishDate 2004
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1470919
http://www.ncbi.nlm.nih.gov/pubmed/15238533
https://doi.org/10.1534/genetics.103.013227
genre Atlantic salmon
genre_facet Atlantic salmon
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1470919
http://www.ncbi.nlm.nih.gov/pubmed/15238533
http://dx.doi.org/10.1534/genetics.103.013227
op_doi https://doi.org/10.1534/genetics.103.013227
container_title Genetics
container_volume 167
container_issue 2
container_start_page 851
op_container_end_page 858
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