CEU cohort

Aliases

CEPH collection, CEPH, Utah residents with ancestry from northern and western Europe, CEU, CEU HapMap, CEU reference panel, CEU reference panels, Central European, European, European (CEU), European ancestry (1KG Phase 1), European population, Europeans, HapMap 2 panel of Utah residents of Northern and Western European ancestry, HapMap CEU sample, HapMap European, HapMap European samples, U.S. Utah residents with ancestry from Northern and Western Europe, Utah Residents with Northern and Western European ancestry, Utah residents of Northern and Western European ancestry, Utah residents with Northern and Western European ancestry, Utah residents with ancestry from northern and western Europe, Utah residents with northern and western European ancestry, simulated CEU HapMap

Related entities (8)

Mentioned in (25)

Papers in which this entity is mentioned.

• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations. (2021)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Genome-wide association study identifies a novel locus for cannabis dependence. (2018)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• A global reference for human genetic variation. (2015)
• Candidate gene-environment interaction research: reflections and recommendations. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• HLA typing from RNA-Seq sequence reads. (2012)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• A new statistic to evaluate imputation reliability. (2010)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)

Merged raw entities (17)

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