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Block network mapping approach to quantitative trait locus analysis
BACKGROUND: Advances in experimental biology have enabled the collection of enormous troves of data on genomic variation in living organisms. The interpretation of this data to extract actionable information is one of the keys to developing novel therapeutic strategies to treat complex diseases. Net...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5178092/ https://www.ncbi.nlm.nih.gov/pubmed/28007037 http://dx.doi.org/10.1186/s12859-016-1351-8 |
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author | Shreif, Zeina Z. Gatti, Daniel M. Periwal, Vipul |
author_facet | Shreif, Zeina Z. Gatti, Daniel M. Periwal, Vipul |
author_sort | Shreif, Zeina Z. |
collection | PubMed |
description | BACKGROUND: Advances in experimental biology have enabled the collection of enormous troves of data on genomic variation in living organisms. The interpretation of this data to extract actionable information is one of the keys to developing novel therapeutic strategies to treat complex diseases. Network organization of biological data overcomes measurement noise in several biological contexts. Does a network approach, combining information about the linear organization of genomic markers with correlative information on these markers in a Bayesian formulation, lead to an analytic method with higher power for detecting quantitative trait loci? RESULTS: Block Network Mapping, combining Similarity Network Fusion (Wang et al., NM 11:333–337, 2014) with a Bayesian locus likelihood evaluation, leads to large improvements in area under the receiver operating characteristic and power over interval mapping with expectation maximization. The method has a monotonically decreasing false discovery rate as a function of effect size, unlike interval mapping. CONCLUSIONS: Block Network Mapping provides an alternative data-driven approach to mapping quantitative trait loci that leverages correlations in the sampled genotypes. The evaluation methodology can be combined with existing approaches such as Interval Mapping. Python scripts are available at http://lbm.niddk.nih.gov/vipulp/. Genotype data is available at http://churchill-lab.jax.org/website/GattiDOQTL. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1351-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5178092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51780922016-12-28 Block network mapping approach to quantitative trait locus analysis Shreif, Zeina Z. Gatti, Daniel M. Periwal, Vipul BMC Bioinformatics Methodology Article BACKGROUND: Advances in experimental biology have enabled the collection of enormous troves of data on genomic variation in living organisms. The interpretation of this data to extract actionable information is one of the keys to developing novel therapeutic strategies to treat complex diseases. Network organization of biological data overcomes measurement noise in several biological contexts. Does a network approach, combining information about the linear organization of genomic markers with correlative information on these markers in a Bayesian formulation, lead to an analytic method with higher power for detecting quantitative trait loci? RESULTS: Block Network Mapping, combining Similarity Network Fusion (Wang et al., NM 11:333–337, 2014) with a Bayesian locus likelihood evaluation, leads to large improvements in area under the receiver operating characteristic and power over interval mapping with expectation maximization. The method has a monotonically decreasing false discovery rate as a function of effect size, unlike interval mapping. CONCLUSIONS: Block Network Mapping provides an alternative data-driven approach to mapping quantitative trait loci that leverages correlations in the sampled genotypes. The evaluation methodology can be combined with existing approaches such as Interval Mapping. Python scripts are available at http://lbm.niddk.nih.gov/vipulp/. Genotype data is available at http://churchill-lab.jax.org/website/GattiDOQTL. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1351-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-22 /pmc/articles/PMC5178092/ /pubmed/28007037 http://dx.doi.org/10.1186/s12859-016-1351-8 Text en © COPYRIGHT NOTICE 2016 The article is a work of the United States Government; Title 17 U.S.C 105 provides that copyright protection is not available for any work of the United States government in the United States. Additionally, this is an open access article distributed under the terms of the Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0), which permits worldwide unrestricted use, distribution, and reproduction in any medium for any lawful purpose. |
spellingShingle | Methodology Article Shreif, Zeina Z. Gatti, Daniel M. Periwal, Vipul Block network mapping approach to quantitative trait locus analysis |
title | Block network mapping approach to quantitative trait locus analysis |
title_full | Block network mapping approach to quantitative trait locus analysis |
title_fullStr | Block network mapping approach to quantitative trait locus analysis |
title_full_unstemmed | Block network mapping approach to quantitative trait locus analysis |
title_short | Block network mapping approach to quantitative trait locus analysis |
title_sort | block network mapping approach to quantitative trait locus analysis |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5178092/ https://www.ncbi.nlm.nih.gov/pubmed/28007037 http://dx.doi.org/10.1186/s12859-016-1351-8 |
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