The phrase "a genotype completion rate" is correct and usable in written English.
It can be used in contexts related to genetics, biology, or research where you are discussing the percentage or rate of completed genotype analyses or assessments.
Example: "The study reported a genotype completion rate of 85%, indicating a high level of participant compliance."
Alternatives: "genotype fulfillment rate" or "genotype assessment rate."
In this final SNP-based edit, six more individuals had a genotype completion rate of <95%.
Ancestry was then determined for the proband by using 5239 widely spaced, independent SNPs that had a genotype completion rate of ≥99.9%.
Ancestry for both Stage 1 and Stage 2 samples was estimated by using 5176 SNPs, which had a genotype completion rate of ≥99.9%, and a minor allele frequency MAF ≥ 0.05 and were separated by at least 500 kb.
We observed a TaqMan® SNP genotype completion rate of >99.55%, an undetermined rate of <0.45%, zero discordant genotypes and zero "no amplification failures" in 7938 attempted TaqMan® SNP genotypes using gDNA template in the TaqMan® SNP assay.
After these exclusions, there were N = 126 tag and singleton SNPs at 30 genes available for analysis with a mean (standard deviation) genotype completion rate of 98.3% (1.1%) [see Additional file 3].
The mass of human DNA added to genotyping reactions was not associated with TaqMan® genotype completion rate (Pearson r = 0.064, P = 0.122), but was significantly associated with VNTR genotype completion rate (Pearson r = 0.173, P < 0.001).
Genotype completion rate was 95%.
gDNA exhibited significantly greater STR genotype completion rate than did 1 ng gDNA input (p < 0.001).
We omitted 12,818 SNPs leaving 40,977 SNPs in our working build of the data and the overall genotype completion rate was 99.8%.
gDNA versus wgaDNA produced from 1 ng gDNA input, SNP genotype completion rates, p < 0.0001.
Concordance between genotype duplicates (n = 12) was 100%, with genotype completion rates of > 89% for SNPs in the mitochondrial genome and > 97.5% for SNPs in the nuclear genome.
