In this vignette, we describe how to use the NewmanOmics Paired and Banked tests to analyze gene expression data from a single sample.
As usual, we start by loading the package:
The package contains paired tumor and normal samples from patients with head and neck cancer. these came from a study that was submitted to the Gene Expression Omnibus.
## [1] 2000 44
## Normal.mucosa.1 Cancer.1 Normal.mucosa.2 Cancer.2
## 34155_s_at 26.42586 22.19725 22.13673 18.66223
## 34281_at 334.29232 382.92879 393.40014 509.30754
## 39125_at 258.62695 290.06060 268.97994 220.16837
## 37276_at 45.65556 38.86692 34.77368 33.40627
## 1519_at 423.26690 366.40731 308.62338 550.34888
As we can see, this consists of (normalized) Affymetrix microarray data. The odd numbered columns are derived from normal mucosa, and the even numbered columns are derived from paired tumor samples.
Before proceeding, we are going to log-transform the data.
Box plot of log-transformed data.
The figure suggests that the the data have been reasonably normalized, and that it is unlikely to be overwhelmed by artifacts.
To illustrate the Newman Paired test, we are going to use only one sample.
## Cancer.1
## Min. :5.842e-04
## 1st Qu.:4.158e-01
## Median :9.885e-01
## Mean :1.417e+00
## 3rd Qu.:1.835e+00
## Max. :1.744e+01
## Cancer.1
## Min. :0.0000
## 1st Qu.:0.3004
## Median :0.5770
## Mean :0.5463
## 3rd Qu.:0.8144
## Max. :0.9997
We can create a histogram of the per-gene (empirical) p-values
Histogram of empoirical p-values.
We can also produce an “M-versus-A” plot of the data.
Bland-Altman plot.
The pairedStat function has flexible inputs, allowing you to store the data in various ways. Here we run the algorithm for three pairs, with an explicit pairing vector.
## Cancer.1 Cancer.2 Cancer.3
## Min. :5.842e-04 Min. :9.836e-04 Min. : 0.001682
## 1st Qu.:4.158e-01 1st Qu.:4.591e-01 1st Qu.: 0.369775
## Median :9.885e-01 Median :1.021e+00 Median : 0.878206
## Mean :1.417e+00 Mean :1.417e+00 Mean : 1.419570
## 3rd Qu.:1.835e+00 3rd Qu.:1.780e+00 3rd Qu.: 1.765563
## Max. :1.744e+01 Max. :1.526e+01 Max. :16.572431
## Cancer.1 Cancer.2 Cancer.3
## Min. :0.0000 Min. :0.0000 Min. :0.0000
## 1st Qu.:0.2999 1st Qu.:0.3150 1st Qu.:0.3187
## Median :0.5773 Median :0.5650 Median :0.6206
## Mean :0.5463 Mean :0.5375 Mean :0.5630
## 3rd Qu.:0.8145 3rd Qu.:0.7957 3rd Qu.:0.8346
## Max. :0.9997 Max. :0.9996 Max. :0.9992
Bland-ALtman plots.
Bland-ALtman plots.
Bland-ALtman plots.
P-value histograms.
P-value histograms.
P-value histograms.
We can also input the same data as a pair of matrices.
normals <- HN[, c(1,3,5)]
tumors <- HN[, c(2,4,6)]
result3 <- pairedStat(normals, tumors)
summary(result3@nu.statistics)## Cancer.1 Cancer.2 Cancer.3
## Min. :5.842e-04 Min. :9.836e-04 Min. : 0.001682
## 1st Qu.:4.158e-01 1st Qu.:4.591e-01 1st Qu.: 0.369775
## Median :9.885e-01 Median :1.021e+00 Median : 0.878206
## Mean :1.417e+00 Mean :1.417e+00 Mean : 1.419570
## 3rd Qu.:1.835e+00 3rd Qu.:1.780e+00 3rd Qu.: 1.765563
## Max. :1.744e+01 Max. :1.526e+01 Max. :16.572431
## Cancer.1 Cancer.2 Cancer.3
## Min. :0.0000 Min. :0.0000 Min. :0.0000
## 1st Qu.:0.3006 1st Qu.:0.3155 1st Qu.:0.3194
## Median :0.5774 Median :0.5652 Median :0.6207
## Mean :0.5465 Mean :0.5377 Mean :0.5632
## 3rd Qu.:0.8151 3rd Qu.:0.7963 3rd Qu.:0.8355
## Max. :0.9998 Max. :0.9996 Max. :0.9993
Or we can input the same data as a list of paired samples.
listOfPairs <- list(HN[,1:2], HN[,3:4], HN[,5:6])
result4 <- pairedStat(listOfPairs)
summary(result4@nu.statistics)## Cancer.1 Cancer.2 Cancer.3
## Min. :5.842e-04 Min. :9.836e-04 Min. : 0.001682
## 1st Qu.:4.158e-01 1st Qu.:4.591e-01 1st Qu.: 0.369775
## Median :9.885e-01 Median :1.021e+00 Median : 0.878206
## Mean :1.417e+00 Mean :1.417e+00 Mean : 1.419570
## 3rd Qu.:1.835e+00 3rd Qu.:1.780e+00 3rd Qu.: 1.765563
## Max. :1.744e+01 Max. :1.526e+01 Max. :16.572431
## Cancer.1 Cancer.2 Cancer.3
## Min. :0.0000 Min. :0.0000 Min. :0.0000
## 1st Qu.:0.3008 1st Qu.:0.3157 1st Qu.:0.3194
## Median :0.5766 Median :0.5641 Median :0.6197
## Mean :0.5461 Mean :0.5374 Mean :0.5628
## 3rd Qu.:0.8141 3rd Qu.:0.7954 3rd Qu.:0.8343
## Max. :0.9997 Max. :0.9996 Max. :0.9992
A completely different approach to personalized transcriptomics is to compare individual samples to a “bank” of known normals.
normals <- HN[, seq(1, ncol(HN), 2)] # odds are normal
tumors <- HN[, seq(2, ncol(HN), 2)] # evens are tumor
bank <- createBank(normals)
result5 <- bankStat(bank, tumors[,1,drop=FALSE])
summary(result5$nu.statistics)## Cancer.1
## Min. :-9.6255
## 1st Qu.:-0.5540
## Median : 0.2797
## Mean : 0.1027
## 3rd Qu.: 0.9911
## Max. : 6.7524
## Cancer.1
## Min. :0.0000
## 1st Qu.:0.2898
## Median :0.6101
## Mean :0.5569
## 3rd Qu.:0.8392
## Max. :1.0000