61 to 70 of 72 Results
Oct 15, 2018
Peil, Barbara; Kabisch, Maria; Fischer, Christine; Hamann, Ute; Lorenzo Bermejo, Justo, 2018, "Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]", https://doi.org/10.11588/data/TT4VM3, heiDATA, V1
The addition of sequence data from own‐study individuals to genotypes from external data repositories, for example, the HapMap, has been shown to improve the accuracy of imputed genotypes. Early approaches for reference panel selection favored individuals who best reflect recombi... |
Oct 15, 2018 -
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]
Adobe PDF - 45.9 KB -
MD5: c2ee1a9e53be3e3e388306df5b2b5415
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Oct 15, 2018 -
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]
R Syntax - 4.4 KB -
MD5: eba2c2916f84dabe389bae2a455dbcbd
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Oct 15, 2018 -
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]
R Syntax - 1.7 KB -
MD5: c1422a5107ff0e5dd33b042cf3c71c61
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Oct 15, 2018
Kesselmeier, Miriam; Lorenzo Bermejo, Justo, 2018, "Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants [Source Code]", https://doi.org/10.11588/data/0Z7H1X, heiDATA, V1
Logistic regression is the most common technique used for genetic case-control association studies. A disadvantage of standard maximum likelihood estimators of the genotype relative risk (GRR) is their strong dependence on outlier subjects, for example, patients diagnosed at unus... |
Oct 15, 2018 -
Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants [Source Code]
MS Word - 88.4 KB -
MD5: d3828960b320592e44fa870b04bb750b
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Oct 15, 2018 -
Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants [Source Code]
Adobe PDF - 116.8 KB -
MD5: 40c189590f4db725e93d70df7636c741
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Oct 5, 2018
Lorenzo Bermejo, Justo; Boekstegers, Felix; González Silos, Rosa; Marcelain, Katherine; Baez Benavides, Pablo; Barahona Ponce, Carol; Müller, Bettina; Ferreccio, Catterina; Koshiol, Jill; Fischer, Christine; Peil, Barbara; Sinsheimer,Janet; Fuentes Guajardo,Macarena; Barajas, Olga; Gonzalez-Jose, Rolando; Bedoya, Gabriel; Cátira Bortolini, Maria; Canizales-Quinteros,Samuel; Gallo, Carla; Ruiz Linares, Andres; Rothhammer, Francisco, 2018, "Subtypes of Native American ancestry and leading causes of death: Mapuche ancestry-specific associations with gallbladder cancer risk in Chile [Dataset]", https://doi.org/10.11588/data/IDSI88, heiDATA, V1
Latin Americans are highly heterogeneous regarding the type of Native American ancestry. Consideration of specific associations with common diseases may lead to substantial advances in unraveling of disease etiology and disease prevention. Here we investigate possible association... |
Plain Text - 256.9 KB -
MD5: c1c28871590259ff73badef8cf1f85ae
Aggregate data (columns are tab-separated, variable names in the first row) |
Plain Text - 35.3 KB -
MD5: b4b74370deb5114cb0cd1b7864e2e0b4
Validation data (columns are tab-separated, variable names in the first row) |