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Little's test of missing data showed that the missing data were MCAR (p = 0.173).
A total of 35 706 SNPs remained after removing SNP with minor allele frequency (MAF) < 0.05 and those that failed the test of missing genotypes (>5 %).
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Note that 5 cases were deleted from the data of 480 total cases for our comparison test because of missing information on their relevant dates.
*2 cases were deleted from the data for our comparison test because of missing information on the relevant dates, and 1 case was deleted because classification as probable case did not occur during the 3 time periods of 2/25 6/15.
A paired samples t-test analysis of missing data revealed a significant reduction between the MSF field test study using the ICAR and the initial pilot study, 8.8% vs. 13.1% respectively, p = .032 (Table 3).
Steroid concentrations in plasma, whole blood, and brain were compared using paired t-tests because of missing data.
Proportions were compared by Mann–Whitney U tests because of missing values when a certain behaviour did not occur at all.
A Mann–Whitney Test was performed to detect differences between the two interfaces while the Little's MCAR test was used to test for randomness of missing data.
The PLINK function test-missing tests the difference of missing rate per SNP between cases and controls.
We found that providers in VA facilities that used additional strategies or systems to prevent missed test results perceived less risk of missing test results.
This procedure was adopted to test the influence of missing data on the results [ 37].
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