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. Author manuscript; available in PMC: 2019 Apr 1.

Published in final edited form as: Cancer. 2018 Apr 1;124(Suppl 7):1583–1589. doi: 10.1002/cncr.31122

TaqMan SNP genotyping assays were performed in triplicate on serum cell-free DNA samples obtained from 26 Hmong individuals. Genotype calls (i.e., C/C, C/G, G/G) were made with TaqMan Genotyper Software (Applied Biosystems) and genotype frequencies were summarized according to A) the three possible genotypes: C/C, C/G, G/G, B) samples with (C/G, G/G) or without (C/C) the “G” allele. C) The genotypes of the entire cohort of samples (in triplicate) are visualized as an allelic discrimination plot.

TaqMan SNP genotyping assays were performed in triplicate on serum cell-free DNA samples obtained from 26 Hmong individuals. Genotype calls (i.e., C/C, C/G, G/G) were made with TaqMan Genotyper Software (Applied Biosystems) and genotype frequencies were summarized according to A) the three possible genotypes: C/C, C/G, G/G, B) samples with (C/G, G/G) or without (C/C) the “G” allele. C) The genotypes of the entire cohort of samples (in triplicate) are visualized as an allelic discrimination plot.