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To explore the potential function of the gut microbiota in the 10 fecal samples we analyzed the microbial metatranscriptomes obtained.
To demonstrate the usefulness of our method to the characterization of complex biological samples, we analyzed the protein composition and post-translational modifications of the Saccaromyces cerevisiae anaphase-promoting complex [25].
For all samples, we analyzed the scans to assess the maximum temperature and the enthalpy of the gel-to-liquid phase transition for each scanning rate.
To test the performance of RP-HILIC in the analysis of highly complex proteomics samples, we analyzed the total protein extract of mouse chondrogenic cells without further purification.
To assess the relative proportion of embryonic versus maternally-derived B6 DNA in our placental samples, we analyzed the methylation status at the IG-DMR, which has been shown to remain differentially methylated in extraembryonic tissue and placenta [ 12, 22].
To compare our findings with what has been observed in clinical samples, we analyzed the expression of PPARγ and hTERT from genome-wide gene expression microarray data for 294 patients [ 32, 40].
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Taking the same agricultural commodity in different markets as samples, we analyze the errors of the time model, the space model, the mixed model in the same time.
For each of the prepared samples, we analyze the absorption profiles of 25 distinct spatial locations, where the spectra are processed as described in section 3.1.
In addition to specific analyses of the BD sample, we analyzed the larger combined sample with the potential of discovering weaker associations; however, there were fewer significant findings in the combined sample, possibly due to larger heterogeneity.
Given the high proportion of UED-holding trainees in the German sample and their small proportion in the Swiss sample, we analyzed the country differences using only the data from trainees without a UED (see Table 6, lower section).
To maximize the probability that 87Sr/86Sr and δD values in feathers were representative of the site in which they were sampled, we analyzed the P1 from marked adults known to have bred at the same site the previous year (n = 6 sites).
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