MAGMA (Maximum Accessible Genome for Mtb Analysis) is a pipeline for comprehensive genomic analyses of Mycobacterium tuberculosis with a focus on clinical decision making as well as research.
- Fine-grained control over resource allocation (CPU/Memory/Storage)
- Reliance of bioconda for installing packages for reproducibility
- Ease of use on a range of infrastructure (cloud/on-prem HPC clusters/ servers (or local machines))
- Resumability for failed processes
- Centralized locations for specifying analysis parameters and hardware requirements
- MAGMA parameters (
default_parameters.config
which can overridden using a params.yaml file) - Hardware requirements (
conf/server.config
orconf/pbs.config
orconf/low_memory.config
) - Execution (software) requirements (
conf/docker.config
orconf/conda_local.config
orconf/podman.config
)
- MAGMA parameters (
git
: The version control in the pipeline.Java-11
orJava-17
LTS release (preferred)
⚠️ Checkjava
version!: Thejava
version should NOT be aninternal jdk
release! You can check the release viajava --version
Notice theLTS
next toOpenJDK
line.
$ java -version
openjdk version "17.0.7" 2023-04-18 LTS
OpenJDK Runtime Environment (build 17.0.7+7-LTS)
OpenJDK 64-Bit Server VM (build 17.0.7+7-LTS, mixed mode, sharing)
- Download Nextflow
$ curl -s https://get.nextflow.io | bash
- Make Nextflow executable
$ chmod +x nextflow
- Add
nextflow
to yourpath
(for example/usr/local/bin/
)
$ mv nextflow /usr/local/bin
- Sanity check for
nextflow
installation
$ nextflow info
Version: 23.04.1 build 5866
Created: 15-04-2023 06:51 UTC (08:51 SAST)
System: Mac OS X 12.6.5
Runtime: Groovy 3.0.16 on OpenJDK 64-Bit Server VM 17.0.7+7-LTS
Encoding: UTF-8 (UTF-8)
✔️ With this you're all set with Nextflow. Next stop, conda or docker - pick one!:
A dummy samplesheet
is provided here
The minimal samplesheet structure should have the following fields.
Sample,R1,R2
S0001,/full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz
S0002,/full_path_to_directory_of_fastq_files/S0002_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0002_01_R2.fastq.gz
S0003,/full_path_to_directory_of_fastq_files/S0003_01_R1.fastq.gz,
If you have the metadata from sequencing instrument, you can specify further information in the samplesheet
Study,Sample,Library,Attempt,R1,R2,Flowcell,Lane,Index Sequence
Study_Name,S0001,1,1,full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz,1,1,1
Study_Name,S0002,1,1,full_path_to_directory_of_fastq_files/S0002_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0002_01_R2.fastq.gz,1,1,1
Study_Name,S0003,1,1,full_path_to_directory_of_fastq_files/S0003_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0003_01_R2.fastq.gz,1,1,1
Study_Name,S0004,1,1,full_path_to_directory_of_fastq_files/S0004_01_R1.fastq.gz,full_path_to_directory_of_fastq_files/S0004_01_R2.fastq.gz,1,1,1
Here's a formatted version of the CSV above, including all optional fields
Study | Sample | Library | Attempt | R1 | R2 | Flowcell | Lane | Index Sequence |
---|---|---|---|---|---|---|---|---|
Study_Name | S0001 | 1 | 1 | full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz | full_path_to_directory_of_fastq_files/S0001_01_R1.fastq.gz | 1 | 1 | 1 |
Study_Name | S0002 | 1 | 1 | full_path_to_directory_of_fastq_files/S0002_01_R1.fastq.gz | full_path_to_directory_of_fastq_files/S0002_01_R2.fastq.gz | 1 | 1 | 1 |
Study_Name | S0003 | 1 | 1 | full_path_to_directory_of_fastq_files/S0003_01_R1.fastq.gz | full_path_to_directory_of_fastq_files/S0003_01_R2.fastq.gz | 1 | 1 | 1 |
Study_Name | S0004 | 1 | 1 | full_path_to_directory_of_fastq_files/S0004_01_R1.fastq.gz | full_path_to_directory_of_fastq_files/S0004_01_R2.fastq.gz | 1 | 1 | 1 |
Note We are currently working on the transition to nf-core standard (see #188), which would add standardized configurations and pipeline structure to benefit from the nf-core nf-core/modules and nf-core/configs projects.
The pipeline parameters are distinct from Nextflow parameters, and therefore it is recommended that they are provided using a yml
file as shown below
# Sample contents of my_parameters_1.yml file
input_samplesheet: /path/to/your_samplesheet.csv
only_validate_fastqs: true
conda_envs_location: /path/to/folder/with/conda_envs
When running the pipeline, use profiles to ensure smooth execution on your computing system. The two types of profiles employed by the pipeline are: execution environment + memory/computing requirements
Execution environment profiles:
- conda_local
- docker
- podman
Memory/computing profiles:
- pbs (good for high performance computing clusters)
- server (good for local servers)
- low_memory (this can be run on a laptop, even limited to 8 cores and 8 GB of RAM)
Advanced Users The MAGMA pipeline has default parameters related to minimum QC thresholds that must be reached for samples to be included in the cohort analysis. These default parameters are listed in default_params.config. Users wishing to adjust these parameters should specify these adjustments in the params.yml file supplied when launching the pipeline. An example of adjusted parameters is shown below: Note The
-profile
mechanism is used to enable infrastructure specific settings of the pipeline. The example below, assumes you are usingconda
based setup.
Which could be provided to the pipeline using -params-file
parameter as shown below
nextflow run 'https://github.com/TORCH-Consortium/MAGMA' \
-profile conda_local, server \
-r v1.1.1 \
-params-file my_parameters_1.yml
You can also use Seqera Platform (aka Nextflow Tower) to run the pipeline on any of the supported cloud platforms and monitoring the pipeline execution.
Please refer the Tower docs for further information.
⚠️ ⚠️ ⚠️ We discourage running MAGMA via conda, it is prone to challenging-to-reproduce errors
You can run the pipeline using Conda, Mamba or Micromamba package managers to install all the prerequisite softwares from popular repositories such as bioconda and conda-forge.
ℹ️ Conda environments and cheatsheet:
You can find out the location of conda environments usingconda env list
. Here's a useful cheatsheet for conda operations.
You can use the conda
based setup for the pipeline for running MAGMA
- On a local linux machine(e.g. your laptop or a university server)
- On an HPC cluster (e.g. SLURM, PBS) in case you don't have access to container systems like Singularity, Podman or Docker
All the requisite softwares have been provided as a conda
recipe (i.e. yml
files)
These files can be downloaded using the following commands
wget https://raw.githubusercontent.com/TORCH-Consortium/MAGMA/master/conda_envs/magma-env-2.yml
wget https://raw.githubusercontent.com/TORCH-Consortium/MAGMA/master/conda_envs/magma-env-1.yml
The conda
environments are expected by the conda_local
profile of the pipeline, it is recommended that it should be created prior to the use of the pipeline, using the following commands. Note that if you have mamba
(or micromamba
) available you can rely upon that instead of conda
.
$ conda env create -n magma-env-1 --file magma-env-1.yml
$ conda env create -n magma-env-2 --file magma-env-2.yml
Once the environments are created, you can make use of the pipeline parameter conda_envs_location
to inform the pipeline of the names and location of the conda envs.
Next, you need to load the WHO Resistance Catalog within tb-profiler
; basically the instructions, which are used to build the necessary containers.
- Download magma_resistance_db_who_v1.zip and unzip it
wget https://github.com/TORCH-Consortium/MAGMA/files/14559680/resistance_db_who_v1.zip
unzip resistance_db_who
- Activate
magma-env-1
, which hastb-profiler
conda activate magma-env-1
- Move inside that folder and use
tb-profiler load_library
functionality to load the database
cd resistance_db_who
tb-profiler load_library ./resistance_db_who
✔️✔️✔️This is the recommended execution strategy
We provide two docker containers with the pipeline so that you could just download and run the pipeline with them. There is NO need to create any docker containers, just download and enable the docker
profile.
🚧 Container build script: The script used to build these containers is provided here.
Although, you don't need to pull the containers manually, but should you need to, you could use the following commands to pull the pre-built and provided containers
docker pull ghcr.io/torch-consortium/magma/magma-container-1:1.1.1
docker pull ghcr.io/torch-consortium/magma/magma-container-2:1.1.1
📝 Have singularity or podman instead?:
If you do have access to Singularity or Podman, then owing to their compatibility with Docker, you can still use the provided docker containers.
Here's the command which should be used
nextflow run 'https://github.com/torch-consortium/magma' \
-params-file my_parameters_2.yml \
-profile docker,pbs \
-r v1.1.1
💡 Hint:
You could use-r
option of Nextflow for working with any specific version/branch of the pipeline.
- HPC based execution for MAGMA, please refer this doc.
- Cloud batch (AWS/Google/Azure) based execution for MAGMA, please refer this doc
In order to run the MAGMA pipeline, you must provide a samplesheet as input. The structure of the samplesheet should be that located in samplesheet
⚠️ Make sure to use full paths!!!:
- Library
Certain samples may have had multiple libraries prepared.
This row allows the pipeline to distinguish between
different libraries of the same sample.
- Attempt
Certain libraries may need to be sequenced multiple times.
This row allows the pipeline to distinguish between
different attempts of the same library.
- Flowcell/Lane/Index Sequence
Providing this information may allow the VQSR filtering step
to better distinguish between true variants and sequencing
errors. Including these is optional, if unknown or irrelevant,
just fill in with a '1' as shown in example_MAGMA_samplesheet.csv)
We also provide some reference GVCF files which you could use for specific use-cases.
-
For small datasets (20 samples or less), we recommend that you download the
EXIT_RIF GVCF
files from https://zenodo.org/record/8054182 containing GVCF reference dataset for ~600 samples is provided for augmenting smaller datasets -
For including Mtb lineages and outgroup (M. canettii) in the phylogenetic tree, you can download the
LineagesAndOutgroup
files from https://zenodo.org/record/8233518
use_ref_gvcf = false
ref_gvcf = "/path/to/FILE.g.vcf.gz"
ref_gvcf_tbi = "/path/to/FILE.g.vcf.gz.tbi"
💡 Custom GVCF dataset:
For creating a custom GVCF dataset, you can refer the discussion here.
Tim Huepink and Lennert Verboven created an in-depth tutorial of the features of the variant calling in MAGMA:
We have also included a presentation (in PDF format) of the logic and workflow of the MAGMA pipeline as well as posters that have been presented at conferences. Please refer the docs folder.
The results directory produced by MAGMA is as follows:
/path/to/results_dir/
.
├── QC_statistics
├── analyses
└── vcf_files
In this directory you will find files related to the quality control carried out by the MAGMA pipeline. The structure is as follows:
/path/to/results_dir/QC_statistics
├── cohort
│ └── multiqc
│ └── multiqc_data
└── per_sample
├── coverage
├── fastqc
└── mapping
- cohort
Here you will find the joint.merged_cohort_stats.tsv
which contains the QC statistics for all samples in the samplesheet and allows users to determine why certain samples failed to be incorporated in the cohort analysis steps
In addition, you'll find the cohort-level MultiQC report generated by per_sample/fastqc
analysis.
- per_sample/coverage
Contains the GATK WGSMetrics outputs for each of the samples in the samplesheet
- per_sample/mapping
Contains the FlagStat and samtools stats for each of the samples in the samplesheet
/path/to/results_dir/analysis
├── cluster_analysis
├── drug_resistance
├── phylogeny
└── snp_distances
- Cluster Analysis
Contains files related to clustering based on 5SNP and 12SNP cutoffs .figtree files: These can be imported directly into Figtree for visualisation
- Drug Resistance
Organised based on the different types of variants as well as combined results:
/path/to/results_dir/analysis/drug_resistance
├── combined_results
├── major_variants
├── minor_variants
└── structural_variants
Each of the directories containing results related to the different variants (major | minor | structural) have text files that can be used to annotate the .treefiles produced by MAGMA in iToL (https://itol.embl.de)
The combined resistance results file contains a per-sample drug resistance summary based on the WHO Catalogue of Mtb mutations (https://www.who.int/publications/i/item/9789240082410)
MAGMA also notes the presence of all variants in in tier 1 and tier 2 drug resistance genes.
- Phylogeny
Contains the outputs of the IQTree phylogenetic tree construction.
📝 By default we recommend that you use the ExDRIncComplex files as MAGMA was optimized to be able to accurately call positions on the edges of complex regions in the Mtb genome
- SNP distances
Contains the SNP distance tables.
📝 By default we recommend that you use the ExDRIncComplex files as MAGMA was optimized to be able to accurately call positions on the edges of complex regions in the Mtb genome
/path/to/results_dir/vcf_files
├── cohort
│ ├── combined_variant_files
│ ├── minor_variants
│ ├── multiple_alignment_files
│ ├── raw_variant_files
│ ├── snp_variant_files
│ └── structural_variants
└── per_sample
├── minor_variants
├── raw_variant_files
└── structural_variants
- Combined variant files
Contains the cohort gvcfs based on major variants detected by the MAGMA pipeline
- Minor variants
Merged vcfs of all samples, generated by LoFreq
- Multiple alignment files
FASTA files for the generation of phylogenetic trees by IQTree
- Raw variant files
Unfiltered indel and SNPs detected by the MAGMA pipeline
- SNP variant files
Filtered SNPs detected by the MAGMA pipeline
- Structural variant files
Unfiltered structural variants detected by the MAGMA pipeline
Contains files related to FASTQ validation and FASTQC analysis
Contains vcf files for major|minor|structural variants for each individual samples
The MAGMA paper has been published here: https://doi.org/10.1371/journal.pcbi.1011648
The XBS variant calling core was published here: https://doi.org/10.1099%2Fmgen.0.000689
Contributions are warmly accepted! We encourage you to interact with us using Discussions and Issues feature of Github.
Please refer the GPL 3.0 LICENSE file.
Here's a quick TLDR for the license terms.