Internal control samples, identified with a unique probe pattern, were also included in each experiment.
Based on spectrophotometric analysis, samples identified with any obvious contamination were purified using modified Qiagen protocols.
Those samples identified with no agglutination (0) were regarded as negative, while those with +, ++ and +++ were regarded as positive.
After genotype calling, samples identified with poor-quality genotype calls, sex errors, or unclear/unexpected sibling relationships were excluded from further analysis; a total of 1,175 samples with available genotype data in both the GWAS and Exome were included in subsequent analysis.
Figure 1 shows a frame from the baseline/highway video sequence of the CDnet dataset [7] and variation of #min for 4 sample pixels identified with colored circles.
Only 37 (6%) women in the whole sample were identified with clinical depression at 12 weeks postpartum (14/297 (5%) in intervention group and 23/315 (7%) in control group).
When detecting the M121I mutation, 42 of 42 mutant samples were identified, with a sensitivity of 100%, and 45 of 47 wild type samples were identified, with a specificity of 95.7%.
Similarly, a metaanalysis of gene expression data from OSCC samples with matched normal samples, identified commonality with our list of 16 genes differentially hypomethylated between tumour and normal tissues.
Samples were identified with suffixes A400 to A650 that represent the annealing temperatures.
The chemical structure of the fabric samples was identified with FTIR spectra.
