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Distributions of nodes identified by MBP and NaV1.6 were indistinguishable, so datasets were pooled for quantitative analysis.
Fifteen publicly available datasets were pooled for a total of 2378 patients, out of whom 1413 were of Caucasian origin (Table 1).
Fifteen publicly available datasets were pooled for a total of 2378 breast cancer patients (whole cohort), out of whom 1413 were of Caucasian origin.
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All of the valid reads from the eight datasets were pooled together for de novo assembly, Trinityrnaseq_r2012-06-08, an assembly program based on the de Bruijn graph theory, and developed specially for transcriptome sequence assembly, was used for paired-end assembly with default or optimal parameters.
The datasets were pooled and checked for normality of distribution by Shapiro Wilk test and compared by nonparametric statistics methods (Friedman ANOVA and Kendall coefficient of concordance; Kruskal Wallis ANOVA).
All five miRNA datasets were pooled (see additional file 3 for details).
The datasets were pooled and thus comprised 7620 respondents from the 2003 NDHS, 33,385 respondents from the 2008 NDHS, and 38,948 respondents for the 2013 NDHS.
Sample weights were applied to correct for small deviations from the age and gender quota requested and the annual datasets were pooled.
To ensure a uniform transcriptome reference across the datasets, all reads were pooled for assembly then the datasets were individually aligned back to the reference transcriptome.
Datasets from 1987 and 2009 were pooled for these analyses.
Therefore, datasets from the replicate experiments were pooled for the purposes of further statistical analysis.
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CEO of Professional Science Editing for Scientists @ prosciediting.com