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Control subjects from the KORA F3 and S4 samples were matched to cases for the German MI Family study 1, Left-main disease and Aachen Heart studies.
Human and chimpanzee samples were matched with respect to sex and relative age as closely as possible, with no sex or age bias shared between the samples used for mRNA and protein measurements (Table S2).
For situation 2, the unique mass classes between the two samples were matched according to the FT MS measured masses (5 ppm error tolerance) and the HRLC elution time (10% variance tolerance).
All brain samples were matched by age (all groups p>0.05, t-test), post mortem delay (all groups p>0.05, t-test), gender (in total 13 males and 12 females and every group consisted of 2 or 3 males), MAPT haplotype (p>0.05, Fischer exact test) and ApoE-ε haplotype (p>0.05, Fischer exact test).
Dust and air samples were matched by city and season.
91 % of the reads from all six samples were matched to transcripts from the assembly set.
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This lack of difference in prevalence rates between unmatched rural and matched samples supports our earlier finding that the matched samples are matched on a set of unfavorable characteristics which are harmful to their nutritional status.
Once the optical density of the standard and NP samples was matched, the PL spectra were recorded and the relative quantum yields of each sample were calculated using the ratio of the areas under their PL spectra.
Situations in which samples are matched are considered.
Normal tissue samples are matched to the anatomic site of the tumor but usually not matched to the participant.
It is important that biomarker samples are matched to samples that provide concurrent measurement of ALT and AST as well.
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