YRI cohort

Aliases

African (YRI), Africans, HapMap African, HapMap YRI, YRI, YRI analysis panels, Yoruba, Yoruba in Ibadan, Nigeria, Yoruba people of Ibadan, Nigeria, Yoruba, Nigeria

Related entities (3)

Mentioned in (18)

Papers in which this entity is mentioned.

• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Global impact of unproductive splicing on human gene expression. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• 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)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• 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)
• Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel). (2016)
• A global reference for human genetic variation. (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)
• Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (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 (7)

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