This is a complete standardized workflow the assembly and subsequent analysis for short-read viral sequencing.
This core workflow is compatible with the illumina artic nf pipeline and produces consensus and variant calls using iVar (1.3) (Grubaugh, 2019) and Freebayes (Garrison, 2012) .
However, it performs far more extensive quality control and visualisation of results including an interactive HTML summary of run results.
Briefly, raw reads undergo qc using fastqc (Andrews) before removal of host-related reads by competitive mapping against a composite host and human reference with BWA-MEM (0.7.5) (Li, 2013), samtools (1.9) (Li, 2009), and a custom script.
This is to ensure raw as data as possible can be deposited in central databases.
After this, reads undergo adapter trimming and further qc with trim-galore (0.6.5) (Martin).
Residual truseq sequencing adapters are then removed through another custom script.
Reads are then mapped to the viral reference with BWA-MEM, and amplicon primer sequences trimmed using ivar (1.3) (Grubaugh, 2019).
Fastqc is then used to perform a QC check on the reads that map to the viral reference.
After this, iVar is used to generate a consensus genome and variants are called using both ivar variants and breseq (0.35) (Deatherage, 2014). Additionally, Freebayes may be run in addition to iVar which will generate a second set of consensus genome(s) and variant call(s) with comparisons made between iVar and FreeBayes to highlight differences in mutation calls.
Coverage statistics are calculated using bedtools before a final QC via quast and a kraken2 taxonomic classification of mapped reads.
Finally, data from all samples are collated via a post-processing script into an interactive summary for exploration of results and quality control.
Optionally, users can run ncov-tools to generate additional quality control and summary plots and statistics.
If you use this software please cite:
Nasir, Jalees A., Robert A. Kozak, Patryk Aftanas, Amogelang R. Raphenya, Kendrick M. Smith, Finlay Maguire, Hassaan Maan et al. "A Comparison of Whole Genome Sequencing of SARS-CoV-2 Using Amplicon-Based Sequencing, Random Hexamers, and Bait Capture." Viruses 12, no. 8 (2020): 895.
https://doi.org/10.3390/v12080895
- Setup Instructions
- SIGNAL Help Screen
- Executing SIGNAL - Summary
- Executing SIGNAL - Detailed
- Run using Docker
- Data summaries
- Pipeline details
git clone --recursive https://github.com/jaleezyy/covid-19-signal
wget https://repo.anaconda.com/miniconda/Miniconda3-latest-Linux-x86_64.sh
bash Miniconda3-latest-Linux-x86_64.sh # follow instructions
source $(conda info --base)/etc/profile.d/conda.sh
conda create -n signal -c conda-forge -c bioconda -c defaults snakemake pandas conda
conda activate signal
There are some issues with conda failing to install newer versions of snakemake
so alternatively install mamba and use that (snakemake has beta support for it within the workflow)
conda install -c conda-forge mamba
mamba create -c conda-forge -c bioconda -n signal snakemake pandas conda
conda activate signal
Additional software dependencies are managed directly by snakemake using conda environment files:
- trim-galore 0.6.5 (docs)
- kraken2 2.1.1 (docs)
- quast 5.0.2 (docs)
- bwa 0.7.17 (docs)
- samtools 1.7/1.9 (docs)
- bedtools 2.26.0 (docs)
- breseq 0.35.0 (docs)
- ivar 1.3 (docs)
- freebayes 1.3.2 (docs)
- pangolin (latest; version can be specified by user) (docs)
- pangolin-data (latest; version can be specified by user; required for Pangolin v4+) (docs)
- pangolearn (latest; version can be specified by user) (docs)
- constellations (latest; version can be specified by user) (docs)
- scorpio (latest; version can be specified by user) (docs)
- pango-designation (latest; version can be specified by user) (docs)
- nextclade (v1.11.0) (docs)
- ncov-tools postprocessing scripts require additional dependencies (see file).
Using the provided signal.py script, the majority of SIGNAL functions can be accessed easily.
To display the help screen:
python signal.py -h
Output:
usage: signal.py [-h] [-c CONFIGFILE] [-d DIRECTORY] [--cores CORES] [--config-only] [--remove-freebayes] [--add-breseq] [-neg NEG_PREFIX] [--dependencies]
[all ...] [postprocess ...] [ncov_tools ...]
SARS-CoV-2 Illumina GeNome Assembly Line (SIGNAL) aims to take Illumina short-read sequences and perform consensus assembly + variant calling for ongoing surveillance and research efforts towards
the emergent coronavirus: Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2).
positional arguments:
all Run SIGNAL with all associated assembly rules. Does not include postprocessing '--configfile' or '--directory' required. The latter will automatically generate a
configuration file and sample table. If both provided, then '--configfile' will take priority
postprocess Run SIGNAL postprocessing on completed SIGNAL run. '--configfile' is required but will be generated if '--directory' is provided
ncov_tools Generate configuration file and filesystem setup required and then execute ncov-tools quality control assessment. '--configfile' is required but will be generated if '--
directory' is provided
optional arguments:
-h, --help show this help message and exit
-c CONFIGFILE, --configfile CONFIGFILE
Configuration file (i.e., config.yaml) for SIGNAL analysis
-d DIRECTORY, --directory DIRECTORY
Path to directory containing reads. Will be used to generate sample table and configuration file
--cores CORES Number of cores. Default = 1
--config-only Generate sample table and configuration file (i.e., config.yaml) and exit. '--directory' required
--remove-freebayes Configuration file generator parameter. Set flag to DISABLE freebayes variant calling (improves overall speed)
--add-breseq Configuration file generator parameter. Set flag to ENABLE optional breseq step (will take more time for analysis to complete)
-neg NEG_PREFIX, --neg-prefix NEG_PREFIX
Configuration file generator parameter. Comma-separated list of negative sontrol sample name(s) or prefix(es). For example, 'Blank' will cover Blank1, Blank2, etc. Recommend
if running ncov-tools. Will be left empty, if not provided
--dependencies Download data dependencies (under a created 'data' directory) required for SIGNAL analysis and exit. Note: Will override other flags! (~10 GB storage required)
signal.py simplies the execution of all functions of SIGNAL. At its simplest, SIGNAL can be run with one line, provided only the directory of sequencing reads.
# Download dependances (only needs to be run once; ~10GB of storage required)
python signal.py --dependencies
# Generate configuration file and sample table (--neg_prefix can be used to note negative controls)
python signal.py --config-only --directory /path/to/reads
# Execute pipeline (step-by-step; --cores defaults to 1 if not provided)
python signal.py --configfile config.yaml --cores NCORES aLL
python signal.py --configfile config.yaml --cores NCORES postprocess
python signal.py --configfile config.yaml --cores NCORES ncov_tools
# ALTERNATIVE
# Execute pipeline (one line)
python signal.py --configfile config.yaml --cores NCORES all postprocess ncov_tools
# ALTERNATIVE
# Execute pipeline (one line; no prior configuration file or sample table steps)
# --directory can be used in place of --configfile to automatically generate a configuration file
python signal.py --directory /path/to/reads --cores NCORES all postprocess ncov_tools
Each of the steps in SIGNAL can be run manually by accessing the individual scripts or running snakemake.
# Download dependances (only needs to be run once; ~10GB of storage required)
bash scripts/get_data_dependencies.sh -d data -a MN908947.3
# Generate sample table
# Modify existing 'example_config.yaml' for your configuration file
bash scripts/generate_sample_table.sh -d /path/to/reads -n sample_table.csv
# Execute pipeline (step-by-step)
snakemake -kp --configfile config.yaml --cores NCORES --use-conda --conda-prefix=$PWD/.snakemake/conda all
snakemake -kp --configfile config.yaml --cores NCORES --use-conda --conda-prefix=$PWD/.snakemake/conda postprocess
snakemake -kp --configfile config.yaml --cores NCORES --use-conda --conda-prefix=$PWD/.snakemake/conda ncov_tools
The pipeline requires:
-
Amplicon primer scheme sequences
-
SARS-CoV2 reference fasta
-
SARS-CoV2 reference gbk
-
SARS-CoV2 reference gff3
-
kraken2 viral database
-
Human GRCh38 reference fasta (for composite human-viral BWA index)
python signal.py --dependencies # defaults to a directory called `data` in repository root OR bash scripts/get_data_dependencies.sh -d data -a MN908947.3 # allows you to rename and relocate the resultant directory
Note: Downloading the database files requires ~10GB of storage, with up to ~35GB required for all temporary downloads!
You can use the --config-only flag to generate both config.yaml and sample_table.csv (see step 4). The directory provided will be used to auto-generate a name for the run.
python signal.py --config-only --directory /path/to/reads
# Outputs: 'reads_config.yaml' and 'reads_sample_table.csv'
You can also create the configuration file through modifying the example_config.yaml to suit your system.
Note: Regardless of method, double-check your configuraation file to ensure the information is correct!
See the example table example_sample_table.csv for an idea of how to organise this table.
Using the --config-only flag, both configuration file and sample table will be generated (see above in step 3) from a given directory path to reads.
Alternatively, you can attempt to use generate_sample_table.sh to circumvent manual creation of the table.
bash scripts/generate_sample_table.sh
Output:
You must specify a data directory containing fastq(.gz) reads.
ASSUMES FASTQ FILES ARE NAMED AS <sample_name>_L00#_R{1,2}*.fastq(.gz)
Flags:
-d : Path to directory containing sample fastq(.gz) files (Absolute paths preferred for consistency, but can use relative paths)
-n : Name or file path for final sample table (with extension) (default: 'sample_table.csv') - will overwrite if file exists
-e : Name or file path for an existing sample table - will append to the end of the provided table
Select one of '-n' (new sample table) or '-e' (existing sample table).
If neither provided, a new sample table called 'sample_table.csv' will be created (or overwritten) by default.
General usage:
# Create new sample table 'sample_table.csv' given path to reads directory
bash scripts/generate_sample_table.sh -d /path/to/reads -n sample_table.csv
# Append to existing sample table 'sample_table.csv' given path to a directory with additional reads
bash scripts/generate_sample_table.sh -d /path/to/more/reads -e sample_table.csv
For the main signal.py script, positional arguments inform the rules of the pipeline to execute with flags supplementing input parameters.
The main rules of the pipeline are as followed:
all= Sequencing pipeline. i.e., take a set of paired reads, perform reference-based assembly to generate a consensus, run lineage assignment, etc.postprocess= Summarize the key results including pangolin lineage, specific mutations, etc, after runningallncov_tools= Create the required conda environment, generate the necessary configuration file, and link needed result files within thencov-toolsdirectory.ncov-toolswill then be executed with output found within the SIGNAL directory.
The generated configuration file from the above steps can be used as input. To run the general pipeline:
python signal.py --configfile config.yaml --cores 4 all
is equivalent to running
snakemake -kp --configfile config.yaml --cores 4 --use-conda --conda-prefix=$PWD/.snakemake/conda all
You can run the snakemake command as written above, but note that if the --conda-prefix is not set as this (i.e., $PWD/.snakemake/conda), then all envs will be reinstalled for each time you change the results_dir in the config.yaml.
Alternatively, you can skip the above configuration and sample table generation steps by simply providing the directory of reads to the main script:
python signal.py --directory /path/to/reads --cores 4 all
A configuartion file and sample table will automatically be generated prior to running SIGNAL all.
FreeBayes variant calling and BreSeq mutational analysis are technically optional tools within the workflow. Using the --directory flag, by default, FreeBayes will run and BreSeq will not. These can be changed by using the --remove-freebayes and --add-breseq flags, respectively.
As with the general pipeline, the generated configuration file from the above steps can be used as input. To run postprocess which summarizes the SIGNAL results:
python signal.py --configfile config.yaml --cores 1 postprocess
is equivalent to running
snakemake -kp --configfile config.yaml --cores 1 --use-conda --conda-prefix=$PWD/.snakemake/conda postprocess
After postprocessing finishes, you'll see the following summary files:
- summary.html top-level summary, with links to per-sample summaries
- {sample_name}/sample.html per-sample summaries, with links for more detailed info
- {sample_name}/sample.txt per-sample summaries, in text-file format instead of HTML
- summary.zip zip archive containing all of the above summary files.
Note that the pipeline postprocessing (snakemake postprocess) is separated from
the rest of the pipeline (snakemake all). This is because in a multi-sample run,
it's likely that at least one pipeline stage will fail. The postprocessing script
should handle failed pipeline stages gracefully, by substituting placeholder values
when expected pipeline output files are absent. However, this confuses snakemake's
dependency tracking, so there seems to be no good alternative to separating piepline
processing and postprocessing into all and postprocess targets.
Related: because pipeline stages can fail, we run (and recommend running if using the snakemake command to run SIGNAL) snakemake all with the -k flag ("Go on with independent jobs if a job fails").
Additionally, SIGNAL can prepare output and execute @jts' ncov-tools to generate phylogenies and alternative summaries.
python signal.py --configfile config.yaml --cores 1 ncov_tools
is equivalent to running
snakemake -kp --configfile config.yaml --cores 1 --use-conda --conda-prefix=$PWD/.snakemake/conda ncov_tools
SIGNAL manages installing the dependencies (within the conda_prefix) and will generate the necessary hard links to required input files from SIGNAL for ncov-tools if it has been cloned as a sub-module (if not found, the script will attempt to pull the submodule) and a fasta containing sequences to include in the tree has been specified using phylo_include_seqs: in the main SIGNAL config.yaml. If run_freebayes is set to True, then SIGNAL will attempt to link the FreeBayes consensus FASTA and variant files, if found. Otherwise, the corresponding iVar files will be used instead.
SIGNAL will then execute ncov-tools and the output will be found within the SIGNAL results directory, specified in SIGNAL's configuration file, under ncov-tools-results. Refer to the ncov-tools documentation for information regarding specific output.
Using signal.py positional arguments, you can specify SIGNAL to perform multiple rules in succession.
python signal.py --configfile config.yaml --cores NCORES all postprocess ncov_tools
In the above command, SIGNAL all, postprocess, and ncov_tools will run using the provided configuration file as input, which links to a sample table.
Note: Regardless of order for positional arguments, or placement of other parameter flags, SIGNAL will always run in the set order priority: all > postprocess > ncov_tools!
If no configuration file or sample table was generated for a run, you can provide --directory with the path to sequencing reads and SIGNAL will auto-generate both required inputs prior to running any rules.
python signal.py --directory /path/to/reads --cores NCORES all postprocess ncov_tools
Overall, this simplifies executing SIGNAL to one line!
Alternatively, the pipeline can be deployed using Docker (see resources/Dockerfile_pipeline for specification).
To pull from dockerhub:
docker pull finlaymaguire/signal
Download data dependencies into a data directory that already contains your reads (data is this example but whatever name you wish to use):
mkdir -p data && docker run -v $PWD/data:/data finlaymaguire/signal:latest bash scripts/get_data_dependencies.sh -d /data
Generate your config.yaml and sample_table.csv (with paths to the readsets underneath /data) and place them into the data directory:
cp config.yaml sample_table.csv $PWD/data
WARNING result_dir in config.yaml must be within /data e.g. /data/results to automatically be copied to your host system. Otherwise they will be automatically deleted when the container finishes running (unless docker is run interactively).
Then execute the pipeline:
docker run -v $PWD/data:/data finlaymaguire/signal conda run -n snakemake snakemake --configfile /data/config.yaml --use-conda --conda-prefix /covid-19-signal/.snakemake/conda --cores 8 all
-
postprocessandncov_toolsas described above generate many summaries including interactive html reports -
To generate summaries of BreSeq among many samples, see how to summarize BreSeq results using gdtools
For a step-by-step walkthrough of the pipeline, see pipeline/README.md.
A diagram of the workflow is shown below (update pending).
