This pipeline uses various statistical tests to identify mRNAs whose expression levels correlated to selected clinical features.
Testing the association between 17733 genes and 5 clinical features across 10 samples, statistically thresholded by Q value < 0.05, 2 clinical features related to at least one genes.
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3 genes correlated to 'AGE'.
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EAF2|55840 , LEMD2|221496 , UBE2E1|7324
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1 gene correlated to 'NEOPLASM.DISEASESTAGE'.
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CFI|3426
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No genes correlated to 'Time to Death', 'PATHOLOGY.T.STAGE', and 'GENDER'.
Complete statistical result table is provided in Supplement Table 1
Table 1. Get Full Table This table shows the clinical features, statistical methods used, and the number of genes that are significantly associated with each clinical feature at Q value < 0.05.
Clinical feature | Statistical test | Significant genes | Associated with | Associated with | ||
---|---|---|---|---|---|---|
Time to Death | Cox regression test | N=0 | ||||
AGE | Spearman correlation test | N=3 | older | N=0 | younger | N=3 |
NEOPLASM DISEASESTAGE | ANOVA test | N=1 | ||||
PATHOLOGY T STAGE | Spearman correlation test | N=0 | ||||
GENDER | t test | N=0 |
Table S1. Basic characteristics of clinical feature: 'Time to Death'
Time to Death | Duration (Months) | 10.2-121.2 (median=26.3) |
censored | N = 6 | |
death | N = 4 | |
Significant markers | N = 0 |
Table S2. Basic characteristics of clinical feature: 'AGE'
AGE | Mean (SD) | 44.2 (16) |
Significant markers | N = 3 | |
pos. correlated | 0 | |
neg. correlated | 3 |
Table S3. Get Full Table List of 3 genes significantly correlated to 'AGE' by Spearman correlation test
SpearmanCorr | corrP | Q | |
---|---|---|---|
EAF2|55840 | -0.9394 | 0 | 0 |
LEMD2|221496 | -0.9394 | 0 | 0 |
UBE2E1|7324 | -0.9394 | 0 | 0 |
Figure S1. Get High-res Image As an example, this figure shows the association of EAF2|55840 to 'AGE'. P value = 0 with Spearman correlation analysis. The straight line presents the best linear regression.

Table S4. Basic characteristics of clinical feature: 'NEOPLASM.DISEASESTAGE'
NEOPLASM.DISEASESTAGE | Labels | N |
STAGE I | 3 | |
STAGE II | 2 | |
STAGE IV | 4 | |
Significant markers | N = 1 |
Table S5. Get Full Table List of one gene differentially expressed by 'NEOPLASM.DISEASESTAGE'
ANOVA_P | Q | |
---|---|---|
CFI|3426 | 1.046e-06 | 0.0182 |
Figure S2. Get High-res Image As an example, this figure shows the association of CFI|3426 to 'NEOPLASM.DISEASESTAGE'. P value = 1.05e-06 with ANOVA analysis.

Table S6. Basic characteristics of clinical feature: 'PATHOLOGY.T.STAGE'
PATHOLOGY.T.STAGE | Mean (SD) | 2.33 (1.3) |
N | ||
1 | 3 | |
2 | 3 | |
4 | 3 | |
Significant markers | N = 0 |
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Expresson data file = ACC-TP.uncv2.mRNAseq_RSEM_normalized_log2.txt
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Clinical data file = ACC-TP.merged_data.txt
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Number of patients = 10
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Number of genes = 17733
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Number of clinical features = 5
For survival clinical features, Wald's test in univariate Cox regression analysis with proportional hazards model (Andersen and Gill 1982) was used to estimate the P values using the 'coxph' function in R. Kaplan-Meier survival curves were plot using the four quartile subgroups of patients based on expression levels
For continuous numerical clinical features, Spearman's rank correlation coefficients (Spearman 1904) and two-tailed P values were estimated using 'cor.test' function in R
For multi-class clinical features (ordinal or nominal), one-way analysis of variance (Howell 2002) was applied to compare the log2-expression levels between different clinical classes using 'anova' function in R
For two-class clinical features, two-tailed Student's t test with unequal variance (Lehmann and Romano 2005) was applied to compare the log2-expression levels between the two clinical classes using 't.test' function in R
For multiple hypothesis correction, Q value is the False Discovery Rate (FDR) analogue of the P value (Benjamini and Hochberg 1995), defined as the minimum FDR at which the test may be called significant. We used the 'Benjamini and Hochberg' method of 'p.adjust' function in R to convert P values into Q values.