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11 to 16 of 16 Results
Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants [Source Code]
Robust logistic regression to narrow down the winner's curse for rare and recessive susceptibility variants [Source Code]
Oct 15, 2018 - Statistical Genetics
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...
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation [Source Code]
Oct 15, 2018 - Statistical Genetics
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...
Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond [Source Code]
Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond [Source Code]
Oct 15, 2018 - Statistical Genetics
Kabisch, Maria; Hamann, Ute; Lorenzo Bermejo, Justo, 2018, "Imputation of Missing Genotypes within LD-Blocks Relying on the Basic Coalescent and Beyond [Source Code]", https://doi.org/10.11588/data/X9UEHB, heiDATA, V1
Background Genotypes not directly measured in genetic studies are often imputed to improve statistical power and to increase mapping resolution. The accuracy of standard imputation techniques strongly depends on the similarity of linkage disequilibrium (LD) patterns in the study...
RNA Sequence Data for Hepatobiliary Cancer Cell Lines
Oct 22, 2018 - Statistical Genetics
Lorenzo Bermejo, Justo et al., 2018, "RNA Sequence Data for Hepatobiliary Cancer Cell Lines", https://doi.org/10.11588/data/SCGJHQ, heiDATA, V1
RNA Sequence Data for Hepatobiliary Cancer Cell Lines
Perfusion quantification data for "Towards Quantitative Perfusion MRI of the Lung in COPD: The Problem of Short-Term Repeatability"
Nov 27, 2018 - Diagnostic and Interventional Radiology
Triphan, Simon, 2018, "Perfusion quantification data for "Towards Quantitative Perfusion MRI of the Lung in COPD: The Problem of Short-Term Repeatability"", https://doi.org/10.11588/data/ZPEZPX, heiDATA, V1, UNF:6:SE0iKbhWdsMOrcUkd706AA== [fileUNF]
ABSTRACT Purpose 4D perfusion magnetic resonance imaging (MRI) with intravenous injection of contrast agent allows for a radiation-free assessment of regional lung function. It is therefore a valuable method to monitor response to treatment in patients with chronic obstructive pu...
3D Focusing in Simple Microfluidic Devices for Continuous-flow Single-cell Imaging [data set]
3D Focusing in Simple Microfluidic Devices for Continuous-flow Single-cell Imaging [data set]
Dec 11, 2018 - KnopLab
Constantinou, Iordania; Jendrusch, Michael; Aspert, Théo; Görlitz, Frederik; Schulze, André; Charvin, Gilles; Knop, Michael, 2018, "3D Focusing in Simple Microfluidic Devices for Continuous-flow Single-cell Imaging [data set]", https://doi.org/10.11588/data/L5J7WO, heiDATA, V1
Accompanying data for the manuscript "3D Focusing in Simple Microfluidic Devices for Continuous-flow Single-cell Imaging".
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