hum0163 Release Note

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Research IDRelease DateType of Data
hum0163.v2 2021/02/09 NGS (NAT2 haplotype)
hum0163.v1 2018/12/14 NGS (Target Capture)

 

hum0163.v2

Genotype frequencies of NAT2 identified from the targeted capture sequencing (NGS) analysis were provided (csv file).

 

hum0163.v1

DNAs extracted from peripheral blood cells of patients with psychiatric/neurological disorders or cancers were used for the targeted NGS analysis focusing on 100 pharmacogenes and CYP2D6. Allele frequencies of 100 pharmacogenes (1846 variants) and genotype frequencies of CYP2D6 for 990 patients were provided (csv file).

Libraries were prepared by using of in-house multiplexPCR and read by Illumina [MiSeq] (paired-end: average read length 377 bp).

 

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