22 research outputs found
Intersect of significant miRs from the adenocarcinoma cases when using non-paired (DESeq) and paired (edgeR) analysis approach.
<p>Adjusted for multiple testing using Benjamini and Hochberg, false discovery rate (FDR) < 0.1. Logarithmic fold change (FC) relative to normal mucosa and FDR from paired analysis using edgeR. miRs also significant in the analysis of the neuroendocrine tumor (NET) is indicated.</p
Figure 2
<p><b>Schematic illustration of statistical approach.</b> Panels A and C show approach using non-paired statistics and the DESeq tool. Panel B shows approach using paired statistics and the edgeR tool. See text for further details.</p
<i>NFKB1</i> mRNA levels in morphologicallynon-affected and affected tissues normalised to the <i>β-actin</i> mRNA level.
<p>NS = not significant.</p>a<p>P-value for the comparison to the expression levels in tissue from healthy individuals using Kruskal Wallis and Dunńs Multiple Comparison test.</p>b<p>P-value for the comparison of the expression levels in normal and affected tissue from the same individual using Paired Student’s t-test.</p
Clinical and histopathological characteristics of patients in the study.
<p>Clinical and histopathological characteristics of patients in the study.</p
Characteristics of study participants.
1<p>There were significantly more males in the group with mild dysplasia and colorectal cancer compared to the group of healthy individuals (p<0.001, Chi squared test).</p>2<p>The age is significant higher among patients with CRC compared to the three other groups (Kruskal-Wallis and Dunn's Multiple Comparison test, p<0.001).</p>3<p>Normal endoscopy.</p
Venn diagram shows the number of significant miRs identified using the non-paired (DESeq) and paired (edgeR) analysis approach.
<p>Venn diagram shows the number of significant miRs identified using the non-paired (DESeq) and paired (edgeR) analysis approach.</p
<i>ABCB1</i> mRNA levels in morphologically normal and affected tissues normalised to the <i>β-actin</i> mRNA level.
<p><i>*P-</i>value <0.05, **<i>P-</i>value <0.01, ***<i>P-</i>value <0.001.</p
<i>NFKB1</i> mRNA levels in morphologically normal and affected tissues normalised to the <i>β-actin</i> mRNA level.
<p>***<i>P-</i>value <0.001.</p
Read classification as predicted by miRanalyzer and miRBase.
<p>Panel A with percentage of sequencing reads mapped to mature miRs (black) of the total reads per experiment. Panel B with number of mature miRs identified per sequencing experiment. The total number of mature human miRs in miRBase release 16 (n = 1212) is included as reference.</p
<i>ABCG2</i> mRNA levels x 10<sup>7</sup> in intestinal tissues normalised to 18S RNA levels
<p><sup>a</sup> P-values for comparison of the expression levels in tissue from healthy individuals adjusted for age and gender.</p><p><sup>b</sup> P value for the comparison of the expression levels in morphologically unaffected and affected tissue from the same individual using Paired Student’s t-test. Matching samples were available from 66 cases with mild-moderate dysplasia, 11 cases with severe dysplasia, and 80 and 83 CRC cases (distant unaffected tissue, and adjacent unaffected tissue, respectively.</p><p><i>ABCG2</i> mRNA levels x 10<sup>7</sup> in intestinal tissues normalised to 18S RNA levels</p