This webpage is for data sharing of 1K Korean human genomes.
For allele frequency data
You can download the allele frequency of SNVs and Indels, Copy Number variants (CNV), Transposable element (TE) insertions of Korea1K genomes for academic purposes. For the method about calling variants, please refer to the publication ( S. Jeon, Y. Bhak, Y. Choi, Y. Jeon, S. Kim, J. Jang, J. Jang, A. Blazyte, C. Kim, Y. Kim, J. Shim, N. Kim, Y. J. Kim, S. G. Park, J. Kim, Y. S. Cho, Y. Park, H.-M. Kim, B.-C. Kim, N.-H. Park, E.-S. Shin, B. C. Kim, D. Bolser, A. Manica, J. S. Edwards, G. Church, S. Lee, J. Bhak, Korean Genome Project: 1094 Korean personal genomes with clinical information. Sci. Adv. 6, eaaz7835 (2020).).
For Raw data and clinical information
Sequencing data (FASTQ), individual genotypes, and clinical data can be provided upon request and document screening, as described in below figure. To request the data, please contact Sungwon Jeon (firstname.lastname@example.org), Jong Bhak (email@example.com).