Abstract

The integrative Japanese Genome Variation Database (iJGVD; http://ijgvd.megabank.tohoku.ac.jp/) provides genomic variation data detected by whole-genome sequencing (WGS) of Japanese individuals. Specifically, the database contains variants detected by WGS of 1,070 individuals who participated in a genome cohort study of the Tohoku Medical Megabank Project. In the first release, iJGVD includes >4,300,000 autosomal single nucleotide variants (SNVs) whose minor allele frequencies are >5.0%.

Highlights

  • The integrative Japanese Genome Variation Database provides genomic variation data detected by whole-genome sequencing (WGS) of Japanese individuals

  • The database contains variants detected by WGS of 1,070 individuals who participated in a genome cohort study of the Tohoku Medical Megabank Project

  • The 1000 Genomes Project (1KGP)[11] involved low-coverage WGS and high-coverage exome sequencing for 41,000 individuals, including 89 Japanese samples, and the data is widely used for genotype imputation

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Summary

Introduction

The integrative Japanese Genome Variation Database (iJGVD; http://ijgvd.megabank.tohoku.ac.jp/) provides genomic variation data detected by whole-genome sequencing (WGS) of Japanese individuals. The database contains variants detected by WGS of 1,070 individuals who participated in a genome cohort study of the Tohoku Medical Megabank Project. IJGVD includes 44,300,000 autosomal single nucleotide variants (SNVs) whose minor allele frequencies are 45.0%.

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