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CalliNGS-NF

A Nextflow pipeline for Variant Calling Analysis with NGS RNA-Seq data based on GATK best practices.

Quickstart

Install Nextflow by using the following command:

curl -s https://get.nextflow.io | bash 

Download the Docker image with this command (optional) :

docker pull cbcrg/callings-nf:gatk4

Launch the pipeline execution with the following command:

nextflow run CRG-CNAG/CalliNGS-NF -profile docker

Note: the Docker image contains all the required dependencies. Add the -profile docker to enable the containerised execution to the example command line shown below.

Pipeline Description

The RNA sequencing (RNA-seq) data, in additional to the expression information, can be used to obtain somatic variants present in the genes of the analysed organism. The CalliNGS-NF pipeline processes RNAseq data to obtain small variants(SNVs), single polymorphisms (SNPs) and small INDELs (insertions, deletions). The pipeline is an implementation of the GATK best practices for variant calling on RNAseq and includes all major steps of the analysis, link.

In addition to the GATK best practics, the pipeline includes steps to compare obtained SNVs with known variants and to calculate allele specific counts for the overlapped SNVs.

Input files

The CalliNGS-NF pipeline needs as the input following files:

• RNAseq reads, *.fastq
• Genome assembly, *.fa
• Known variants, *.vcf
• Denylisted regions of the genome, *.bed

The RNAseq read file names should match the following naming convention: sampleID{1,2}_{1,2}.extension

where:

• sampleID is the identifier of the sample;
• the first number 1 or 2 is the replicate ID;
• the second number 1 or 2 is the read pair in the paired-end samples;
• extension is the read file name extension eg. fq, fq.gz, fastq.gz, etc.

example: ENCSR000COQ1_2.fastq.gz.

Pipeline parameters

--reads

• Specifies the location of the reads FASTQ file(s).
• Multiple files can be specified using the usual wildcards (*, ?), in this case make sure to surround the parameter string value by single quote characters (see the example below)
• By default it is set to the CalliNGS-NF's location: $baseDir/data/reads/rep1_{1,2}.fq.gz
• See above for naming convention of samples, replicates and pairs read files.

Example:

$ nextflow run CRG-CNAG/CalliNGS-NF --reads '/home/dataset/*_{1,2}.fq.gz'

--genome

• The location of the genome fasta file.
• It should end in .fa.
• By default it is set to the CalliNGS-NF's location: $baseDir/data/genome.fa.

Example:

$ nextflow run CRG-CNAG/CalliNGS-NF --genome /home/user/my_genome/human.fa

--variants

• The location of the known variants VCF file.
• It should end in .vcf or vcf.gz.
• By default it is set to the CalliNGS-NF's location: $baseDir/data/known_variants.vcf.gz.

Example:

$ nextflow run CRG-CNAG/CalliNGS-NF --variants /home/user/data/variants.vcf

--denylist (formely --blacklist)

• The location of the denylisted genome regions in bed format.
• It should end in .bed.
• By default it is set to the CalliNGS-NF's location: $baseDir/data/denylist.bed.

Example:

$ nextflow run CRG-CNAG/CalliNGS-NF --denylist /home/user/data/denylisted_regions.bed

--results

• Specifies the folder where the results will be stored for the user.
• It does not matter if the folder does not exist.
• By default is set to CalliNGS-NF's folder: results

Example:

$ nextflow run CRG-CNAG/CalliNGS-NF --results /home/user/my_results

Pipeline results

For each sample the pipeline creates a folder named sampleID inside the directory specified by using the --results command line option (default: results). Here is a brief description of output files created for each sample:

Schematic Outline

Requirements

• Nextflow 20.07.1 (or later)
• Java 8 or later
• Docker 1.10 (or later) or Singularity engine
• GATK 4.1.x

Note: CalliNGS-NF can be used without a container engine by installing in your system all the required software components reported in the following section. See the included Dockerfile for the configuration details.

Components

CalliNGS-NF uses the following software components and tools:

• Java 8
• Samtools 1.3.1
• Vcftools 0.1.14
• STAR 2.5.2b
• GATK 4.1
• R 3.1.1
• Awk
• Perl
• Grep