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Type 1 samples represent iron oxide-rich samples with possible mixture of iron oxides and sulfides.
We validated the assay for EGFR exon 19 in a series of 10 samples with possible sequence verified exon 19 deletions and a tumor percentage of more than 50%.
Samples with possible null alleles were regenotyped, and the data were re-examined using Micro-Checker 2.2.3.
For those types of samples with possible RNA degradation, consistent application of the RIN ≥ 7.0 cutoff is useful for obtaining high quality gene expression microarray data.
From any samples with possible follicular immunoreactivity, we prepared 12 additional 4 µm sections and three 10 µm paraffin rolls (fig 1).
Population structure was assessed by multidimensional scaling (MDS) analysis (using 100 000 random SNPs), removing outlying samples with possible recent non-Norwegian ancestry.
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Furthermore, admixture was common within each sample, with possible membership in >1 cluster for the majority of samples.
The response rate of 58% does not reflect the practices of over 40% of the initial sample, with possible systematic differences between respondents and non-respondents in terms of the nature and level of consumer involvement.
In the first step, the user would define a "sample group", with possible values assigned to each sample in the dataset appropriately.
As discussed below, the goal of having samples with largest possible number of detected substances is likely to have biased the data towards samples that represent more stressed waters.
The obtained amplification curves from unpurified DNA samples with all possible outcomes for each probe are shown in Figure 1.
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