BioWDL: RNA-seq

A BioWDL pipeline for processing RNA-seq data, starting with FASTQ files to produce expression measures and VCFs.

Please be aware that the page you are currently viewing is not for the latest available version!

This pipeline can be used to process RNA-seq data, starting from FastQ files. It will perform quality control (using FastQC and MultiQC), adapter clipping (using cutadapt), mapping (using STAR or HISAT2) and expression quantification and transcript assembly (using HTSeq-Count and Stringtie). Optionally variantcalling (based on the GATK Best Practises) and lncRNA detection (using CPAT) can also be performed.

This pipeline is part of BioWDL developed by the SASC team at Leiden University Medical Center.

Usage

This pipeline can be run using Cromwell

First download the latest version of the pipeline wdl file and zip imports package from the releases page.

The pipeline can then be run with the following command:

java -jar cromwell-<version>.jar run \
  -o options.json \
  -i inputs.json \
  --imports RNA-seq_v<version>.zip \
  RNA-seq_<version>.wdl

Where options.json contains the following json:

{
  "final_workflow_outputs_dir": "/path/to/outputs",
  "use_relative_output_paths": true,
}

The options.json will make sure all outputs end up in /path/to/outputs in an easy to navigate folder structure.

Dependency requirements and tool versions

Biowdl pipelines use docker images to ensure reproducibility. This means that biowdl pipelines will run on any system that has docker installed. Alternatively they can be run with singularity.

For more advanced configuration of docker or singularity please check the cromwell documentation on containers.

Images from biocontainers are preferred for biowdl pipelines. The list of default images for this pipeline can be found in the default for the dockerImages input.

Inputs

Inputs are provided through a JSON file. The minimally required inputs are described below, but additional inputs are available. A template containing all possible inputs can be generated using Womtool as described in the WOMtool documentation. For an overview of all available inputs, see this page.

{
  "RNAseq.sampleConfigFile":"The sample configuration file. See below for more details.",
  "RNAseq.dockerImagesFile": "A file listing the used docker images.",
  "RNAseq.starIndex": "A list of star index files.",
  "RNAseq.referenceFasta": "A path to a reference fasta",
  "RNAseq.referenceFastaFai": "The path to the index associated with the reference fasta",
  "RNAseq.referenceFastaDict": "The path to the dict file associated with the reference fasta",
  "RNAseq.refflatFile": "Reference annotation Refflat file. This will be used for expression quantification.",
  "RNAseq.referenceGtfFile": "Reference annotation GTF file. This will be used for expression quantification.",
  "RNAseq.strandedness": "Indicates the strandedness of the input data. This should be one of the following: FR (Forward, Reverse), RF (Reverse, Forward) or None: (Unstranded)"
}

If you wish to use hisat2 instead, set the list of hisat2 index files on RNAseq.hisat2Index.

If neither a starIndex nor a hisat2Index is provided, then a STAR index will be generated on the fly using the provided GTF file and reference Fasta.

The referenceGtfFile may also be omitted, in this case Stringtie will be used to perform an unguided assembly, which will then be used for expression quantification.

Optional settings:

{
  "RNAseq.adapterForward": "Used to set a forward read adapter. Default: Illumina Universal Adapter  AGATCGGAAGAG",
  "RNAseq.adapterReverse": "Used to set a reverse read adapter (for paired-end reads). Default: Illumina Universal Adapter  AGATCGGAAGAG",
  "RNAseq.umiDeduplication": "Whether or not UMI based deduplication should be run. See the notes below on UMIs.",
  "RNAseq.scatterSizeMillions": "The size of the scattered regions in million bases for the GATK subworkflows. Scattering is used to speed up certain processes. The genome will be seperated into multiple chunks (scatters) which will be processed in their own job, allowing for parallel processing. Higher values will result in a lower number of jobs. The optimal value here will depend on the available resources."
}

UMIs are expected to have been extracted from the input fastq files and added to the headers of the reads. A tool like UMI-tools may be used to do so. Please be aware that different library preparation protocols will put the UMIs in different locations in your reads, so be careful when extracting the UMIs!

Sample configuration

Verification

All samplesheet formats can be verified using biowdl-input-converter. It can be installed with pip install biowdl-input-converter or conda install biowdl-input-converter (from the bioconda channel). Python 3.7 or higher is required.

With biowdl-input-converter --validate samplesheet.csv The file “samplesheet.csv” will be checked. Also the presence of all files in the samplesheet will be checked to ensure no typos were made. For more information check out the biowdl-input-converter readthedocs page.

CSV Format

The sample configuration can be given as a csv file with the following columns: sample, library, readgroup, R1, R1_md5, R2, R2_md5.

column name function
sample sample ID
library library ID. These are the libraries that are sequenced. Usually there is only one library per sample
readgroup readgroup ID. Usually a library is sequenced on multiple lanes in the sequencer, which gives multiple fastq files (referred to as readgroups). Each readgroup pair should have an ID.
R1 The fastq file containing the first reads of the read pairs
R1_md5 Optional: md5sum for the R1 file.
R2 Optional: The fastq file containing the second reads of the read pairs
R2_md5 Optional: md5sum for the R2 file

The easiest way to create a samplesheet is to use a spreadsheet program such as LibreOffice Calc or Microsoft Excel, and create a table:

sample library readgroup R1 R1_md5 R2 R2_md5
sample1 lib1 rg1 data/s1-l1-rg1-r1.fastq      
sample2 lib1 rg1 data/s1-l1-rg1-r2.fastq      

NOTE: R1_md5, R2 and R2_md5 are optional do not have to be filled. And additional fields may be added (eg. for documentation purposes), these will be ignored by the pipeline.

After creating the table in a spreadsheet program it can be saved in csv format.

YAML format

The sample configuration can also be a YML file which adheres to the following structure:

samples:
  - id: <sampleId>
    libraries:
      - id: <libId>
        readgroups:
          - id: <rgId>
            reads:
              R1: <Path to first-end FastQ file.>
              R1_md5: <MD5 checksum of first-end FastQ file.>
              R2: <Path to second-end FastQ file.>
              R2_md5: <MD5 checksum of second-end FastQ file.>

Replace the text between < > with appropriate values. MD5 values may be omitted and R2 values may be omitted in the case of single-end data. Multiple readgroups can be added per library and multiple libraries may be given per sample.

Variantcalling

In order to perform variant calling the following inputs are also required:

{
  "RNAseq.variantCalling": "Whether or not variantcalling should be performed, defaults to False",
  "RNAseq.dbsnpVCF": "A VCF file to aid in the variantcalling",
  "RNAseq.dbsnpVCFIndex": "The index for the dbsnpVCF"
}

And these settings are optional when variant calling is performed:

{
  "RNAseq.variantCallingRegions": "A BED file that describes the regions where variants should be called"
}

lncRNA detection

In order to perform lncRNA detection the following inputs are also required:

{
  "RNAseq.lncRNAdetection": "Whether or not lncRNA detection should be performed, defaults to False",
  "RNAseq.lncRNAdatabases": "A list of gtf files containing known lncRNAs",
  "RNAseq.cpatLogitModel": "The CPAT logitModel to be used",
  "RNAseq.cpatHex": "The CPAT hexamer tab file to be used"
}

Example

The following is an example of what an inputs JSON might look like:

{
 "RNAseq.sampleConfigFile":"/home/user/analysis/samples.yml",
  "RNAseq.starIndex": [
    "/reference/star/chrLength.txt",
    "/reference/star/chrName.txt",
    "/reference/star/chrNameLength.txt",
    "/reference/star/chrStart.txt",
    "/reference/star/Genome",
    "/reference/star/genomeParameters.txt",
    "/reference/star/SA",
    "/reference/star/SAindex"
  ],
  "RNAseq.variantCalling": true,
  "RNAseq.lncRNAdetection": true,
  "RNAseq.referenceFasta": "/home/user/genomes/human/GRCh38.fasta",
  "RNAseq.referenceFastaFai": "/home/user/genomes/human/GRCh38.fasta.fai",
  "RNAseq.referenceFastaDict": "/home/user/genomes/human/GRCh38.dict",
  "RNAseq.dbsnpVCF": "/home/user/genomes/human/dbsnp/dbsnp-151.vcf.gz",
  "RNAseq.dbsnpVCFIndex": "/home/user/genomes/human/dbsnp/dbsnp-151.vcf.gz.tbi",
  "RNAseq.lncRNAdatabases": ["/home/user/genomes/human/NONCODE.gtf"],
  "RNAseq.cpatLogitModel": "/home/user/genomes/human/GRCH38_logit",
  "RNAseq.cpatHex": "/home/user/genomes/human/GRCH38_hex.tab",
  "RNAseq.refflatFile": "/home/user/genomes/human/GRCH38_annotation.refflat",
  "RNAseq.gtfFile": "/home/user/genomes/human/GRCH38_annotation.gtf",
  "RNAseq.strandedness": "RF",
  "RNAseq.dockerImagesFile": "dockerImages.yml"
}

And the associated samplesheet might look like this:

sample library readgroup R1 R1_md5 R2 R2_md5
patient1 lib1 lane1 /home/user/data/patient1/R1.fq.gz 181a657e3f9c3cde2d3bb14ee7e894a3 /home/user/data/patient1/R2.fq.gz ebe473b62926dcf6b38548851715820e
patient2 lib1 lane1 /home/user/data/patient2/lane1_R1.fq.gz 7e79b87d95573b06ff2c5e49508e9dbf /home/user/data/patient2/lane1_R2.fq.gz dc2776dc3a07c4f468455bae1a8ff872
patient2 lib1 lane2 /home/user/data/patient2/lane2_R1.fq.gz 18e9b2fef67f6c69396760c09af8e778 /home/user/data/patient2/lane2_R2.fq.gz 72209cc64510827bc3f849bab00dfe7d

Saved as csv format it will look like this.

"sample","library","readgroup","R1","R1_md5","R2","R2_md5"
"patient1","lib1","lane1","/home/user/data/patient1/R1.fq.gz","181a657e3f9c3cde2d3bb14ee7e894a3","/home/user/data/patient1/R2.fq.gz","ebe473b62926dcf6b38548851715820e"
"patient2","lib1","lane1","/home/user/data/patient2/lane1_R1.fq.gz","7e79b87d95573b06ff2c5e49508e9dbf","/home/user/data/patient2/lane1_R2.fq.gz","dc2776dc3a07c4f468455bae1a8ff872"
"patient2","lib1","lane2","/home/user/data/patient2/lane2_R1.fq.gz","18e9b2fef67f6c69396760c09af8e778","/home/user/data/patient2/lane2_R2.fq.gz","72209cc64510827bc3f849bab00dfe7d"

The pipeline also supports tab- and ;-delimited files.

Output

This pipeline will produce a number of directories and files:

Contact

For any question about running this pipeline and feature requests, please use the github issue tracker or contact the SASC team directly at: sasc@lumc.nl.