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1 to 10 of 16 Results
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...
Subtypes of Native American ancestry and leading causes of death: Mapuche ancestry-specific associations with gallbladder cancer risk in Chile [Dataset]
Oct 5, 2018 - Statistical Genetics
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...
Statistical Genetics(Heidelberg University - Medical Faculty Heidelberg)
Oct 5, 2018
Data publications from the Statistical Genetics Group at Heidelberg University's Institute of Medical Biometry and Informatics.
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...
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
Raw data and analysis scripts for "Design and application of an MR reference phantom for multicentre lung imaging trials"
Jun 8, 2018 - Diagnostic and Interventional Radiology
Triphan, Simon; Biederer, Jürgen; Burmester, Kerstin; Fellhauer, Iven; Vogelmeier, Claus; Jörres, Rudolf; Kauczor, Hans-Ulrich; Heußel, Claus; Wielpütz, Mark; Jobst, Bertram, 2018, "Raw data and analysis scripts for "Design and application of an MR reference phantom for multicentre lung imaging trials"", https://doi.org/10.11588/data/FHOCRZ, heiDATA, V1
This dataset contains all MRI phantom data discussed in the related publication as well as the python scripts used to analyse them. The format is DICOM files, where institution names and adresses have been anonymized. Abstract Introduction: As there is an increasing number of mul...
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...
Mittelalterliche Pflanzenreste von der Marktstätte und Brotlaube in Konstanz [Dataset]
Mittelalterliche Pflanzenreste von der Marktstätte und Brotlaube in Konstanz [Dataset]
Jul 18, 2018 - Propylaeum@heiDATA
Küster, Hansjörg, 2018, "Mittelalterliche Pflanzenreste von der Marktstätte und Brotlaube in Konstanz [Dataset]", https://doi.org/10.11588/data/ARWJHB, heiDATA, V1
During excavations in medieval Konstanz very many samples were taken for archaeobotanical analyses. Samples could be dated to different time layers from High to Late Middle Ages. Spelt, millet and oats were probably the most important cereals. But also flax, hemp, figs and spices...
Mapping degradation signals and pathways in a eukaryotic N-terminome [data set]
Mar 5, 2018 - KnopLab
Kats, Ilia; Khmelinskii, Anton; Kschonsak, Marc; Huber, Florian; Knieß, Robert A.; Bartosik, Anna; Knop, Michael, 2018, "Mapping degradation signals and pathways in a eukaryotic N-terminome [data set]", https://doi.org/10.11588/data/9ZQIKF, heiDATA, V1
Data accompanying the paper "Mapping degradation signals and pathways in a eukaryotic N-terminome".
Institute of Pathology Mannheim(Heidelberg University - Medical Faculty Mannheim)
May 18, 2018
Data publications from the Institute of Pathology Mannheim at the Medical Faculty Mannheim (Heidelberg University).
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