Sentence examples for population frequency between from inspiring English sources

The weaker version implies that the OR of every risk allele with a population frequency between 0.04 and 0.945 is less than 1.50 ( Table 5).

The standard version of the criterion B implies that the OR of every risk allele with a population frequency between 0.05 and 0.95 is less than 1.04 ( Table 4).

The statistical significance of the difference in population frequency between FL and TR elements was significant in the Gulf Atlantic population (P < 0.01), and highly significant in the Suwannee and Central Florida populations (P < 0.001).

Indeed, more than 2.9 million case control pairs should be recruited to a GWAS to identify a susceptibility variant of a population frequency between 0.0005 and 0.9995 with a power of 0.8 (Appendix C).

In this study, we considered all remaining CNVs (with frequency >0.1%, refered as 'all CNVs') and we also distinguished between Copy Number Polymorphisms ('CNPs', CNVs with a frequency greater than 1% in the population) and the remaining ones (i.e. CNVs with population frequency between 0.1% and 1%) to which we refer as Copy Number Variant Regions ('CNVRs').

If the mutation rate at a putative risk locus is relatively low μ = 1.48 × 10 − 6, more than 290 million case control pairs are required in a GWAS to detect a risk variant of a population frequency between 0.000005 and 0.999995 with a power of 0.8 (Appendix C).

More tellingly, the five losing clones were virtually eliminated from the low relatedness populations (mean summed population frequency 0.0054).

For the parametric linkage analysis (PLA) we assumed a dominant model with a susceptibility allele with population frequency 0.003.

If these populations were intermediates on the way to the dominance of QS49 (red) seen in the high relatedness populations, we would expect to see even fewer of these loser clones at high relatedness, but in fact we see many more (mean summed population frequency 0.093).

We analyzed the combined GBM and LGG (low grade glioma) datasets from the TCGA (n = 542 samples) and identified 128 genes that are mutated (non-silent mutations only) in ten or more samples, consistent with a population frequency >1.7 % (i.e. 10/542 = 1.8%%).

When we compared our copy-number frequencies with copy-number frequencies in a study (2) reporting integer copy numbers for each of the overlapping CNV regions, the frequencies were fairly close to each other [60% of the CNV regions had lower than 0.05 in the total variation distance between population frequencies (11, 32)].