hum0015 Release Note

Research IDRelease DateType of Data
hum0015.v3 2019/01/11 Allele frequencies of SNVs and In/dels on autosomal chromosomes, X-chromosome and mitochondrial DNA in 3552 participants
hum0015.v2 2018/12/27 Allele frequencies of SNVs and In/dels on autosomal chromosomes, X-chromosome and mitochondrial DNA in 3552 participants
hum0015.v1 2014/10/14 Frequencies of known autosomal SNPs whose minor allele frequencies are more than 5% in 1070 participants.

 

hum0015.v3

The access level of JGAD00000000159 (Controlled Access [Type I]) was changed to "Un-restricted Access" (hum0015.v3.3.5kjpnv2.v1).

 

hum0015.v2

Whole-genome sequencing by using of HiSeq 2500 was performed. After genotype calling for each individual, genotypes of 3552 individuals were pooled, and allele frequencies were calculated. Allele frequencies of SNVs and Indels on autosomal chromosomes, X-chromosome, and mitochondrial DNA in 3552 participants were provided.

 

hum0015.v1

Whole-genome sequencing by using of HiSeq 2500 was performed. After genotype calling for each individual, genotypes of 1070 individuals were pooled, and allele frequencies were calculated. Autosomal SNPs (minor allele frequency > 5%) that matched known SNPs in dbSNP138 were selected.

 

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