Identifying the genetic basis of complex traits remains an important and challenging problem with the potential to affect a broad range of biological endeavors. A number of statistical methods are available for mapping quantitative trait loci (QTL), but their application to high-throughput phenotypes has been limited as most require user input and interaction. Recently, methods have been developed specifically for expressionQTL (eQTL) mapping, but they too are limited in that they do not allow for interactions and QTL of moderate effect. We here propose an automated model-selection-based approach that identifies multiple eQTL in experimental populations, allowing for eQTL of moderate effect and interactions. Output can be used to identify groups of transcripts that are likely coregulated, as demonstrated in a study of diabetes in mouse.
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Univ Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USAUniv Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USA
Zhuang, Yonghua
Wade, Kristen
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Univ Colorado, Sch Med, Human Med Genet & Genom Program, Anschutz Med Campus, Aurora, CO 80045 USAUniv Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USA
Wade, Kristen
Saba, Laura M.
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Univ Colorado, Skaggs Sch Pharm & Pharmaceut Sci, Dept Pharmaceut Sci, Anschutz Med Campus, Aurora, CO 80045 USAUniv Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USA
Saba, Laura M.
Kechris, Katerina
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Univ Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USAUniv Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus,Mail Stop B119, Aurora, CO 80045 USA
机构:Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
Kompass, Kenneth S.
Witte, John S.
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Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
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Univ Wisconsin, Dept Stat, Madison, WI 53706 USAUniv Wisconsin, Dept Stat, Madison, WI 53706 USA
Quoc Tran
Broman, Karl W.
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Univ Wisconsin, Dept Biostat & Med Informat, 2126 Genet Biotechnol Ctr,425 Henry Mall, Madison, WI 53706 USAUniv Wisconsin, Dept Stat, Madison, WI 53706 USA
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S China Agr Univ, Guangdong Key Lab Plant Mol Breeding, Guangzhou 510642, Guangdong, Peoples R ChinaNanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R China
Liu, G. F.
Li, M.
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Nanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R ChinaNanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R China
Li, M.
Wen, J.
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Nanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R ChinaNanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R China
Wen, J.
Du, Y.
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Nanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R ChinaNanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R China
Du, Y.
Zhang, Y. -M.
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Nanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R ChinaNanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Sect Stat Genom, Nanjing 210095, Peoples R China