HapMap3 cohort

Aliases

CEU founder population, HapMap, HapMap 3, HapMap Phase 3, HapMap SNP, HapMap3

Related entities (1)

Mentioned in (18)

Papers in which this entity is mentioned.

• Specificity, length and luck drive gene rankings in association studies. (2026)
• MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. (2016)
• HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
• HLA typing from 1000 genomes whole genome and whole exome illumina data. (2013)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• Integrative analysis of the melanoma transcriptome. (2010)
• Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)

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