3.6. 61KJPN-SNV/INDEL
- Dataset category
Genome Variation
- Overview
SNV/INDEL allele frequency and genotype frequency data obtained from short-read whole genome sequencing of about 61,000 Japanese individuals
- References
Tadaka et al. [2]
- Samples analyzed
Blood (buffy coat), saliva
- Number of samples (by analysis platform)
Analysis platform
Male
Female
Total
Illumina HiSeq 2500 (162PE)
1,314
1,559
2,873
Illumina HiSeq 2500 (259PE) *1
107
174
281
Illumina HiSeq X Five (150PE) *1
31
34
65
Illumina NovaSeq 6000 (150PE) *2
4,209
14,271
18,480
Illumina NovaSeq 6000 (151PE) *2
1,495
2,224
3,719
Illumina NovaSeq 6000 (161PE)
9,182
15,415
24,597
Illumina NovaSeq X Plus (161PE)
922
2,553
3,475
MGI DNBSeq G400 (150PE) *1
528
560
1,088
MGI DNBSeq T7 (150PE)
2,954
3,892
6,846
Total
20,742
40,682
61,424
[1] Due to the small sample size, frequency information is not displayed on the jMorp Web site and in the downloadable files.
[2] On the jMorp Web site and in downloadable files, 150PE and 151PE are combined and referred to as 150PE.
- Number of samples (by age)
Age
Male
Female
Total
19 and below
726
724
1,440
20s
1,347
5,851
7,198
30s
3,263
10,398
13,661
40s
1,862
3,780
5,642
50s
2,143
5,471
7,614
60s
7,525
10,635
18,160
70s
3,770
3,742
7,512
over 80
106
81
187
Total
20,742
40,682
61,424
- Related pages on the jMorp website