African cohort

Aliases

AFR, African, African ancestry, African individuals, African population, African samples, Africans

Related entities (5)

Mentioned in (35)

Papers in which this entity is mentioned.

• Mapping the genetic landscape across 14 psychiatric disorders. (2026)
• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Efficient and accurate search in petabase-scale sequence repositories. (2025)
• OXSeg: Multidimensional Attention UNet-Based Lip Segmentation Using Semi-Supervised Lip Contours. (2025)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
• KILDA: identifying KIV-2 repeats from kmers. (2025)
• BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
• MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
• Principles and methods for transferring polygenic risk scores across global populations. (2024)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• A harmonized public resource of deeply sequenced diverse human genomes. (2024)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
• AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Rare variant phasing using paired tumor:normal sequence data. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• 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)
• 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)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
• The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• A new statistic to evaluate imputation reliability. (2010)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

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