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Meningioma samples were chosen as disease control group.
The four samples were chosen, because they showed an intense Cu signal in the inked areas.
Two samples were chosen from each of the six M. tuberculosis lineages.
C-F patient samples were chosen so that the full spectrum of Bacteroidetes phylum abundance was represented.
Replicated miRNAs were averaged and miRNAs that intensities > = 30 in all samples were chosen for calculating normalization factor.
Four wine samples were chosen: table red, oloroso, tawny port and rosé.
The specific surface areas of the activated samples were chosen for the selected process response.
These samples were chosen to present a challenge of indenting at small loads (μN range).
The probability of same clonal features for different samples decreases 50% with one sample increase, especially all samples were chosen randomly.
Samples were chosen to include the widest possible range of haplogroup R1a-M582 internal variation based on their previously available short tandem repeat (STR) haplotypes (Supplemental Table S2).
Two different MQW samples were chosen for measurements.
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