# ROSeq

Modeling expression ranks for noise-tolerant differential expression analysis of scRNA-Seq data

## Introduction

ROSeq - A rank based approach to modeling gene expression with filtered and normalized read count matrix. ROSeq takes filtered and normalized read matrix and cell-annotation/condition as input and determines the differentially expressed genes between the contrasting groups of single cells. One of the input parameters is the number of cores to be used.

## Installation

The developer’s version of the R package can be installed with the following R commands:

    if (!requireNamespace("BiocManager", quietly = TRUE))
        install.packages("BiocManager")

    # The following initializes usage of Bioc devel
    BiocManager::install(version='devel')

    BiocManager::install("ROSeq")

The github’s version of the R package can be installed with the following R commands:

    library(devtools)
    install_github('krishan57gupta/ROSeq')

## Vignette tutorial

This vignette uses the Tung dataset, which is already inbuilt in the package, to demonstrate a standard pipeline.

## Example

Libraries need to be loaded before running.

    library(ROSeq)
    library(edgeR)
    #> Loading required package: limma
    library(limma)

### Loading tung dataset

    samples<-list()
    samples$count<-ROSeq::L_Tung_single$NA19098_NA19101_count
    samples$group<-ROSeq::L_Tung_single$NA19098_NA19101_group
    samples$count[1:5,1:5]
    #>                 NA19098.r1.A01 NA19098.r1.A02 NA19098.r1.A03 NA19098.r1.A04
    #> ENSG00000237683              0              0              0              1
    #> ENSG00000187634              0              0              0              0
    #> ENSG00000188976              3              6              1              3
    #> ENSG00000187961              0              0              0              0
    #> ENSG00000187583              0              0              0              0
    #>                 NA19098.r1.A05
    #> ENSG00000237683              0
    #> ENSG00000187634              0
    #> ENSG00000188976              4
    #> ENSG00000187961              0
    #> ENSG00000187583              0

### Data Preprocessing:

#### Cells and genes filtering then voom transformation after TMM normalization

Below commands can be used for Cell/gene filtering, TMM normalization and voom transformation. The user is free to use an alternative preprocessing strategy while using different filtering/normalization methods.

    gene_names<-rownames(samples$count)
    samples$count<-apply(samples$count,2,function(x) as.numeric(x))
    rownames(samples$count)<-gene_names
    samples$count<-samples$count[,colSums(samples$count> 0) > 2000]
    gkeep<-apply(samples$count,1,function(x) sum(x>2)>=3)
    samples$count<-samples$count[gkeep,]
    samples$count<-limma::voom(ROSeq::TMMnormalization(samples$count))

### ROSeq analysis.

Input: gene expression matrix with genes in rows and cells in columns. Condition/group annotation of cells also need to be supplied. User can set numCores based the hardware specifications in her computer.

    output<-ROSeq(countData=samples$count$E, condition = samples$group, numCores=1)

### Showing results are in the form of pVals and pAdj

##### p_Vals : p_value (unadjusted)

##### p_Adj : Adjusted p-value, based on FDR method

    output[1:5,]
    #>                     pVals      pAdj
    #> ENSG00000237683 0.6741426 0.9321651
    #> ENSG00000188976 0.7484244 0.9426495
    #> ENSG00000187608 0.2282451 0.8481636
    #> ENSG00000188157 0.5138812 0.9082800
    #> ENSG00000131591 0.1235577 0.7438811