JPT cohort

Aliases

HapMap JPT, Japanese, Japanese from Tokyo, Japanese in Tokyo, Japanese in Tokyo, Japan, unrelated individuals from Tokyo, Japan

Related entities (13)

Mentioned in (21)

Papers in which this entity is mentioned.

• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
• A global reference for human genetic variation. (2015)
• A global reference for human genetic variation. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Genetic structure of Europeans: a view from the North-East. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• Marker selection for genetic case-control association studies. (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 (6)

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