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A similarity matrix of samples was generated by treating each age class as an individual variable.
The FE mesh of digital samples was generated with the locations of image pixels within each aggregate and asphalt matrix.
A similar recognition pattern to all sera and vaginal washes samples was generated by the two variants of HBcAg, also similar to a pool of human anti-HBcAg positive sera.
The second set of samples was generated from unstimulated whole blood culture as described above.
First, a list of genes (number = 838) differentially expressed (2-fold or more change in expression levels) between DM and control samples was generated.
For clonal bisulfite pyrosequencing, PCR product from individual samples was generated by non-biotinated primers (Table S2) and subsequently TA-cloned into pGEM-Teasy vector (Promega).
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Paired samples were generated for each patient.
Point samples are generated according to the importance sampling function.
First, numerous solution samples are generated and tested.
Discrete samples were generated as shown in Table 7.
The clutter samples were generated with the extracted correlation properties.
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