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A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content

Using the Genetic Analysis Workshop 14 (GAW14) simulated dataset, we compare microsatellite and single-nucleotide polymorphism (SNP) markers in terms of two measures of information content, the traditional entropy-based information content measure, and a new "relative information" measure....

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Autores principales: Thalamuthu, Anbupalam, Mukhopadhyay, Indranil, Ray, Amrita, Weeks, Daniel E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866759/
https://www.ncbi.nlm.nih.gov/pubmed/16451636
http://dx.doi.org/10.1186/1471-2156-6-S1-S27
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author Thalamuthu, Anbupalam
Mukhopadhyay, Indranil
Ray, Amrita
Weeks, Daniel E
author_facet Thalamuthu, Anbupalam
Mukhopadhyay, Indranil
Ray, Amrita
Weeks, Daniel E
author_sort Thalamuthu, Anbupalam
collection PubMed
description Using the Genetic Analysis Workshop 14 (GAW14) simulated dataset, we compare microsatellite and single-nucleotide polymorphism (SNP) markers in terms of two measures of information content, the traditional entropy-based information content measure, and a new "relative information" measure. Both attempt to measure the amount of information contained in the markers about the identity-by-descent (IBD) sharing among relatives. The performance of the two information measures are compared based on their variability and ability to predict change in the LOD score (ΔLOD) as map density increases for SNP markers. Although in a linked region, LOD scores are correlated with measures of information, we observe that none of the measures predict the LOD score itself very well. In an unlinked region, the LOD score is not related to either measures of information. The information content of microsatellite markers with 7.5-cM spacing is slightly higher than that of SNP markers with 3-cM spacing. At these map densities, microsatellites are found to be uniformly more informative than SNPs irrespective of their level of heterozygosity. For SNPs, we found that as the level of heterozygosity increases, the information content increases. As reported in all other previous studies, we also found that high-density SNPs have higher information content compared to low-density microsatellites. Performance of both the two information measures considered here are similar, but the relative information measure predicts ΔLOD as marker density increases better than the traditional entropy-based information measure.
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spelling pubmed-18667592007-05-11 A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content Thalamuthu, Anbupalam Mukhopadhyay, Indranil Ray, Amrita Weeks, Daniel E BMC Genet Proceedings Using the Genetic Analysis Workshop 14 (GAW14) simulated dataset, we compare microsatellite and single-nucleotide polymorphism (SNP) markers in terms of two measures of information content, the traditional entropy-based information content measure, and a new "relative information" measure. Both attempt to measure the amount of information contained in the markers about the identity-by-descent (IBD) sharing among relatives. The performance of the two information measures are compared based on their variability and ability to predict change in the LOD score (ΔLOD) as map density increases for SNP markers. Although in a linked region, LOD scores are correlated with measures of information, we observe that none of the measures predict the LOD score itself very well. In an unlinked region, the LOD score is not related to either measures of information. The information content of microsatellite markers with 7.5-cM spacing is slightly higher than that of SNP markers with 3-cM spacing. At these map densities, microsatellites are found to be uniformly more informative than SNPs irrespective of their level of heterozygosity. For SNPs, we found that as the level of heterozygosity increases, the information content increases. As reported in all other previous studies, we also found that high-density SNPs have higher information content compared to low-density microsatellites. Performance of both the two information measures considered here are similar, but the relative information measure predicts ΔLOD as marker density increases better than the traditional entropy-based information measure. BioMed Central 2005-12-30 /pmc/articles/PMC1866759/ /pubmed/16451636 http://dx.doi.org/10.1186/1471-2156-6-S1-S27 Text en Copyright © 2005 Thalamuthu 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 Proceedings
Thalamuthu, Anbupalam
Mukhopadhyay, Indranil
Ray, Amrita
Weeks, Daniel E
A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title_full A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title_fullStr A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title_full_unstemmed A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title_short A comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
title_sort comparison between microsatellite and single-nucleotide polymorphism markers with respect to two measures of information content
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866759/
https://www.ncbi.nlm.nih.gov/pubmed/16451636
http://dx.doi.org/10.1186/1471-2156-6-S1-S27
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