This vignette provides the necessary instructions for performing the Partial Correlation coefficient with Information Theory (PCIT) (Reverter and Chan 2008) and Regulatory Impact Factors (RIF) (Reverter et al. 2010) algorithm.

The PCIT algorithm identifies meaningful correlations to define edges in a weighted network and can be applied to any correlation-based network including but not limited to gene co-expression networks, while the RIF algorithm identify critical transcript factors (TF) from gene expression data.

These two algorithms when combined provide a very relevant layer of information for gene expression studies (Microarray, RNA-seq and single-cell RNA-seq data).

A gene expression data from microarray, RNA-seq or single-cell RNA-seq spanning two biological conditions of interest (e.g. normal/tumor, healthy/disease, malignant/nonmalignant) is subjected to standard normalization techniques and significance analysis to identify the target genes whose expression is differentially expressed (DE) between the two conditions. Then, the regulators (e.g. Transcript Factors genes) are identified in the data. The TF genes can be obtained from the literature (Wang and Nishida 2015)(Vaquerizas et al. 2009). Next, the co-expression correlation between each TF and the DE genes is computed for each of the two conditions. This allows for the computation of the differential wiring (DW) from the difference in co-expression correlation existing between a TF and a DE genes in the two conditions. As a result, RIF analysis assigns an extreme score to those TF that are consistently most differentially co-expressed with the highly abundant and highly DE genes (case of RIF1 score), and to those TF with the most altered ability to act as predictors of the abundance of DE genes (case of RIF2 score). A given TF may not show a change in expression profile between the two conditions to score highly by RIF as long as it shows a big change in co-expression with the DE genes. To this particular, the profile of the TF gene (triangle, solid line) is identical in both conditions (slightly downwards). Instead, the DE gene (circle, dashed line) is clearly over-expressed in condition B. Importantly, the expression of the TF and the DE gene shows a strong positive correlation in condition A, and a strong negative correlation in condition B.

The proposed PCIT algorithm contains two distinct steps as follows:

For every trio of genes in x, y and z, the three first-order partial correlation coefficients are computed by:

\[r_{xy.z} = \frac{r_{xy} - r_{xz} r_{yz}}{\sqrt{(1-r^{2}_{xz})(1-r^{2}_{yz})}}\], and similarly for \(r_{xz.y}\) and \(r_{yz.x}\).

The partial correlation coefficient between *x* and *y* given *z* (here denoted by \(r_{xy.z}\)) indicates the strength of the linear relationship between *x* and *y* that is independent of (uncorrelated with) *z*. Calculating the ordinary (or unconditional or zero-order) correlation coefficient and comparing it with the partial correlation, we might see that the association between the two variables has been sharply reduced after eliminating the effect of the third variable.

We invoke the Data Processing Inequality (DPI) theorem of Information Theory which states that ‘no clever manipulation of the data can improve the inference that can be made from the data’ (Cover and Thomas 2012). For every trio of genes, and in order to obtain the tolerance level (\(\varepsilon\)) to be used as the local threshold for capturing significant associations, the average ratio of partial to direct correlation is computed as follows:

\[\varepsilon = (\frac{r_{xy.z}}{r_{xy}} + \frac{r_{xz.y}}{r_{xz}} + \frac{r_{yz.x}}{r_{yz}})\] In the context of our network reconstruction, a connection between genes *x* and *y* is discarded if:

\[|r_{xy}| \le |\varepsilon r_{xz}| and |r_{xy}| \le |\varepsilon r_{yz}|\] Otherwise, the association is defined as significant, and a connection between the pair of genes is established in the reconstruction of the GCN. To ascertain the significance of the association between genes *x* and *y*, the above mentioned Steps 1 and 2 are repeated for each of the remaining *n−2* genes (denoted here by *z*).

To install, just type:

for Linux users is necessary to install **libcurl4-openssl-dev**, **libxml2-dev** and **libssl-dev** dependencies.

There are many ways to perform the analysis. The following sections will be splited by steps, and finishing with the complete analysis with visualization. We will use the **airway** (Himes et al. 2014) dataset in the following sections. This dataset provides a RNA-seq count data from four human ASM cell lines that were treated with dexamenthasone - a potent synthetic glucocorticoid. Briefly, this dataset has 4 samples untreated and other 4 samples with the treatment.

The first option is to perform the PCIT analysis. The output will be a list with 3 elements. The first one contains a dataframe with the pairwise correlation between genes (corr1) and the significant pairwise correlation (corr2 \(\neq\) 0). The second element of the list stores the adjacency matrix with all correlation. And the last element contains the adjacency matrix with only the significant values:

```
# Loading packages
library(CeTF)
library(airway)
library(kableExtra)
library(knitr)
# Loading airway data
data("airway")
# Creating a variable with annotation data
anno <- as.data.frame(colData(airway))
anno <- anno[order(anno$dex, decreasing = TRUE), ]
anno <- data.frame(cond = anno$dex,
row.names = rownames(anno))
# Creating a variable with count data
counts <- assay(airway)
# Sorting count data samples by conditions (untrt and trt)
counts <- counts[, rownames(anno)]
colnames(counts) <- paste0(colnames(counts), c(rep("_untrt", 4), rep("_trt", 4)))
# Differential Expression analysis to use only informative genes
DEGenes <- expDiff(exp = counts,
anno = anno,
conditions = c('untrt', 'trt'),
lfc = 4.5,
padj = 0.05,
diffMethod = "Reverter")
# Selecting only DE genes from counts data
counts <- counts[rownames(DEGenes$DE_unique), ]
# Converting count data to TPM
tpm <- apply(counts, 2, function(x) {
(1e+06 * x)/sum(x)
})
# Count normalization
PCIT_input <- normExp(tpm)
# PCIT input for untrt
PCIT_input_untrt <- PCIT_input[,grep("_untrt", colnames(PCIT_input))]
# PCIT input for trt
PCIT_input_trt <- PCIT_input[,grep("_trt", colnames(PCIT_input))]
# Performing PCIT analysis for untrt condition
PCIT_out_untrt <- PCIT(PCIT_input_untrt, tolType = "mean")
# Performing PCIT analysis for trt condition
PCIT_out_trt <- PCIT(PCIT_input_trt, tolType = "mean")
# Printing first 10 rows for untrt condition
kable(PCIT_out_untrt$tab[1:10, ]) %>%
kable_styling(bootstrap_options = "striped", full_width = FALSE)
```

gene1 | gene2 | corr1 | corr2 |
---|---|---|---|

ENSG00000011465 | ENSG00000026025 | 0.01160 | 0.00000 |

ENSG00000011465 | ENSG00000035403 | 0.61286 | 0.00000 |

ENSG00000011465 | ENSG00000049323 | -0.71685 | 0.00000 |

ENSG00000011465 | ENSG00000067225 | -0.99935 | -0.99935 |

ENSG00000011465 | ENSG00000071127 | -0.56817 | 0.00000 |

ENSG00000011465 | ENSG00000071242 | -0.89063 | 0.00000 |

ENSG00000011465 | ENSG00000075624 | 0.09820 | 0.00000 |

ENSG00000011465 | ENSG00000077942 | -0.80938 | 0.00000 |

ENSG00000011465 | ENSG00000080824 | -0.72639 | 0.00000 |

ENSG00000011465 | ENSG00000087086 | -0.91357 | 0.00000 |

```
# Printing first 10 rows for trt condition
kable(PCIT_out_trt$tab[1:10, ]) %>%
kable_styling(bootstrap_options = "striped", full_width = FALSE)
```

gene1 | gene2 | corr1 | corr2 |
---|---|---|---|

ENSG00000011465 | ENSG00000026025 | 0.63800 | 0.00000 |

ENSG00000011465 | ENSG00000035403 | 0.96857 | 0.96857 |

ENSG00000011465 | ENSG00000049323 | 0.14794 | 0.00000 |

ENSG00000011465 | ENSG00000067225 | -0.99687 | -0.99687 |

ENSG00000011465 | ENSG00000071127 | -0.92734 | -0.92734 |

ENSG00000011465 | ENSG00000071242 | -0.75914 | 0.00000 |

ENSG00000011465 | ENSG00000075624 | -0.70489 | 0.00000 |

ENSG00000011465 | ENSG00000077942 | -0.29712 | 0.00000 |

ENSG00000011465 | ENSG00000080824 | -0.93148 | 0.00000 |

ENSG00000011465 | ENSG00000087086 | -0.94620 | 0.00000 |

After performing the PCIT analysis, it is possible to verify the histogram distribution of the clustering coefficient of the adjacency matrix with the significant values:

It’s possible to generate the density plot with the significance values of correlation. We’ll use the raw adjacency matrix and the adjacency matrix with significant values. It is necessary to define a cutoff of the correlation module (values between -1 and 1) that will be considered as significant:

To perform the RIF analysis we will need the count data, an annotation table and a list with the Transcript Factors of specific organism (*Homo sapiens* in this case) and follow the following steps in order to get the output (dataframe with the average expression, RIF1 and RIF2 metrics for each TF):

```
# Loading packages
library(CeTF)
library(airway)
library(kableExtra)
library(knitr)
# Loading airway data
data("airway")
# Creating a variable with annotation data
anno <- as.data.frame(colData(airway))
anno <- anno[order(anno$dex, decreasing = TRUE), ]
anno <- data.frame(cond = anno$dex,
row.names = rownames(anno))
# Creating a variable with count data
counts <- assay(airway)
# Sorting count data samples by conditions (untrt and trt)
counts <- counts[, rownames(anno)]
colnames(counts) <- paste0(colnames(counts), c(rep("_untrt", 4), rep("_trt", 4)))
# Differential Expression analysis to use only informative genes
DEGenes <- expDiff(exp = counts,
anno = anno,
conditions = c('untrt', 'trt'),
lfc = 2,
padj = 0.05,
diffMethod = "Reverter")
# Selecting only DE genes from counts data
counts <- counts[rownames(DEGenes$DE_unique), ]
# Converting count data to TPM
tpm <- apply(counts, 2, function(x) {
(1e+06 * x)/sum(x)
})
# Count normalization
Clean_Dat <- normExp(tpm)
# Loading the Transcript Factors (TFs) character
data("TFs")
# Verifying which TFs are in the subsetted normalized data
TFs <- rownames(Clean_Dat)[rownames(Clean_Dat) %in% TFs]
# Selecting the Target genes
Target <- setdiff(rownames(Clean_Dat), TFs)
# Ordering rows of normalized count data
RIF_input <- Clean_Dat[c(Target, TFs), ]
# Performing RIF analysis
RIF_out <- RIF(input = RIF_input,
nta = length(Target),
ntf = length(TFs),
nSamples1 = 4,
nSamples2 = 4)
# Printing first 10 rows
kable(RIF_out[1:10, ]) %>%
kable_styling(bootstrap_options = "striped", full_width = FALSE)
```

TF | avgexpr | RIF1 | RIF2 |
---|---|---|---|

ENSG00000008441 | 10.380590 | -0.1386859 | -0.6770894 |

ENSG00000102804 | 9.264843 | 0.0147001 | 0.1789910 |

ENSG00000103888 | 13.591598 | 0.0985383 | -0.3361795 |

ENSG00000103994 | 10.385093 | -1.2748364 | 0.8113721 |

ENSG00000112837 | 8.143177 | -0.2246323 | -1.7903370 |

ENSG00000116016 | 11.376028 | -1.2315044 | 0.0216295 |

ENSG00000116132 | 9.388008 | 1.4038890 | 0.8823288 |

ENSG00000118689 | 9.189257 | 0.9971123 | 0.3981473 |

ENSG00000123562 | 9.207009 | 0.3381318 | 0.4609342 |

ENSG00000157514 | 7.215664 | -1.5628941 | -0.3290858 |

Finally, it is possible to run the entire analysis all at once. The output will be a CeTF object with all results generated between the different steps. To access the CeTF object is recommended to use the accessors from **CeTF** class:

```
# Loading packages
library(airway)
library(CeTF)
# Loading airway data
data("airway")
# Creating a variable with annotation data
anno <- as.data.frame(colData(airway))
# Creating a variable with count data
counts <- assay(airway)
# Sorting count data samples by conditions (untrt and trt)
counts <- counts[, order(anno$dex, decreasing = TRUE)]
# Loading the Transcript Factors (TFs) character
data("TFs")
# Performing the complete analysis
out <- runAnalysis(mat = counts,
conditions=c("untrt", "trt"),
lfc = 5,
padj = 0.05,
TFs = TFs,
nSamples1 = 4,
nSamples2= 4,
tolType = "mean",
diffMethod = "Reverter",
data.type = "counts")
```

Based on CeTF class object resulted from **runAnalysis** function is possible to get a plot for Differentially Expressed (DE) genes that shows the relationship between log(baseMean) and Difference of Expression or log2FoldChange, enabling the visualization of the distribution of DE genes and TF in both conditions. These two first plot provides a initial graphical visualization of results:

```
# Using the runAnalysis output (CeTF class object)
SmearPlot(object = out,
diffMethod = 'Reverter',
lfc = 1.5,
conditions = c('untrt', 'trt'),
type = "DE")
```

Then is possible to generate the same previous plot but now for a single TF. So, if you have a specific TF that you want to visualize, this is the recommended plot:

```
# Using the runAnalysis output (CeTF class object)
SmearPlot(object = out,
diffMethod = 'Reverter',
lfc = 1.5,
conditions = c('untrt', 'trt'),
TF = 'ENSG00000185917',
label = TRUE,
type = "TF")
```

```
## Warning: ggrepel: 1 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps
```

The next output is a network for both conditions resulted from :

```
## Warning: The `<scale>` argument of `guides()` cannot be `FALSE`. Use "none" instead as
## of ggplot2 3.3.4.
## ℹ The deprecated feature was likely used in the CeTF package.
## Please report the issue to the authors.
```