Results 11 to 20 of about 199,171 (299)

Comparing Multiple Imputation Methods to Address Missing Patient Demographics in Immunization Information Systems: Retrospective Cohort Study

open access: yesJMIR Public Health and Surveillance
BackgroundImmunization Information Systems (IIS) and surveillance data are essential for public health interventions and programming; however, missing data are often a challenge, potentially introducing bias and impacting the accuracy of vaccine coverage
Sara Brown   +5 more
doaj   +2 more sources

Evaluation of Multi-parameter Test Statistics for Multiple Imputation

open access: goldMultivariate Behavioral Research, 2017
In Ordinary Least Square regression, researchers often are interested in knowing whether a set of parameters is different from zero. With complete data, this could be achieved using the gain in prediction test, hierarchical multiple regression, or an omnibus F test. However, in substantive research scenarios, missing data often exist. In the context of
Yu Liu, Craig K. Enders
openalex   +3 more sources

Accurate and adaptive imputation of summary statistics in mixed-ethnicity cohorts [PDF]

open access: hybridBioinformatics, 2018
Abstract Motivation Methods based on summary statistics obtained from genome-wide association studies have gained considerable interest in genetics due to the computational cost and privacy advantages they present.
Matteo Togninalli   +3 more
openalex   +3 more sources

xQTLImp: efficient and accurate xQTL summary statistics imputation [PDF]

open access: gold, 2019
AbstractMotivationQuantitative trait locus (QTL) analysis of multiomic molecular traits, such as gene transcription (eQTL), DNA methylation (mQTL) and histone modification (haQTL), has been widely used to infer the effects of genomic variation on multiple levels of molecular activities.
Tao Wang   +5 more
openalex   +2 more sources

Advanced Statistics: Missing Data in Clinical Research—Part 2: Multiple Imputation [PDF]

open access: bronzeAcademic Emergency Medicine, 2007
In part 1 of this series, the authors describe the importance of incomplete data in clinical research, and provide a conceptual framework for handling incomplete data by describing typical mechanisms and patterns of censoring, and detailing a variety of relatively simple methods and their limitations.
Craig D. Newgard, Jason S. Haukoos
openalex   +3 more sources

Improved imputation of summary statistics for admixed populations [PDF]

open access: gold, 2017
AbstractMotivationSummary statistics imputation can be used to infer association summary statistics of an already conducted, genotype-based meta-analysis to higher ge-nomic resolution. This is typically needed when genotype imputation is not feasible for some cohorts.
Sina Rüeger   +2 more
openalex   +2 more sources

Methods for Addressing Missingness in Electronic Health Record Data for Clinical Prediction Models: Comparative Evaluation

open access: yesJMIR Medical Informatics
BackgroundMissing data are a common challenge in electronic health record (EHR)–based prediction modeling. Traditional imputation methods may not suit prediction or machine learning models, and real-world use requires workflows that are implementable for
Jean Digitale   +4 more
doaj   +2 more sources

Statistical Inference for Chi-square Statistics or F-Statistics Based on Multiple Imputation [PDF]

open access: green
Missing data is a common issue in medical, psychiatry, and social studies. In literature, Multiple Imputation (MI) was proposed to multiply impute datasets and combine analysis results from imputed datasets for statistical inference using Rubin's rule. However, Rubin's rule only works for combined inference on statistical tests with point and variance ...
Binhuan Wang, Yixin Fang, Man Jin
openalex   +3 more sources

An empirical evaluation of imputation accuracy for association statistics reveals increased type-I error rates in genome-wide associations [PDF]

open access: diamondBMC Genetics, 2011
Background Genome wide association studies (GWAS) are becoming the approach of choice to identify genetic determinants of complex phenotypes and common diseases.
Pereira Alexandre C   +4 more
doaj   +2 more sources

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