nf-core/mhcquant
Identify and quantify MHC eluted peptides from mass spectrometry raw data
2.2.0
). The latest
stable release is
2.6.0
.
Introduction
nfcore/mhcquant is a bioinformatics analysis pipeline used for quantitative processing of data dependent (DDA) peptidomics data.
It was specifically designed to analyse immunopeptidomics data, which deals with the analysis of affinity purified, unspecifically cleaved peptides that have recently been discussed intensively in the context of cancer vaccines.
The workflow is based on the OpenMS C++ framework for computational mass spectrometry. RAW files (mzML) serve as inputs and a database search (Comet) is performed based on a given input protein database. FDR rescoring is applied using Percolator based on a competitive target-decoy approach (reversed decoys). For label free quantification all input files undergo identification based retention time alignment (MapAlignerIdentification), and targeted feature extraction matching ids between runs (FeatureFinderIdentification). In addition, a variant calling file (vcf) can be specified to translate variants into proteins that will be included in the database search and binding predictions on specified alleles (alleles.tsv) using MHCFlurry (Class 1) or MHCNugget (Class 2) can be directly run on the output peptide lists. Moreover, if a vcf file was specified, neoepitopes will automatically be determined and binding predictions can also directly be predicted for them.
The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It uses Docker/Singularity containers making installation trivial and results highly reproducible. The Nextflow DSL2 implementation of this pipeline uses one container per process which makes it much easier to maintain and update software dependencies. Where possible, these processes have been submitted to and installed from nf-core/modules in order to make them available to all nf-core pipelines, and to everyone within the Nextflow community!
On release, automated continuous integration tests run the pipeline on a full-sized dataset on the AWS cloud infrastructure. This ensures that the pipeline runs on AWS, has sensible resource allocation defaults set to run on real-world datasets, and permits the persistent storage of results to benchmark between pipeline releases and other analysis sources. The results obtained from the full-sized test can be viewed on the nf-core website.
Pipeline summary
- Present QC for raw reads (
MultiQC
)
(This chart was created with the help of Lucidchart)
Quick Start
-
Install
Nextflow
(>=21.10.3
) -
Install any of
Docker
,Singularity
,Podman
,Shifter
orCharliecloud
for full pipeline reproducibility (please only useConda
as a last resort; see docs) -
Download the pipeline and test it on a minimal dataset with a single command:
Note that some form of configuration will be needed so that Nextflow knows how to fetch the required software. This is usually done in the form of a config profile (
YOURPROFILE
in the example command above). You can chain multiple config profiles in a comma-separated string.- The pipeline comes with config profiles called
docker
,singularity
,podman
,shifter
,charliecloud
andconda
which instruct the pipeline to use the named tool for software management. For example,-profile test,docker
. - Please check nf-core/configs to see if a custom config file to run nf-core pipelines already exists for your Institute. If so, you can simply use
-profile <institute>
in your command. This will enable eitherdocker
orsingularity
and set the appropriate execution settings for your local compute environment. - If you are using
singularity
and are persistently observing issues downloading Singularity images directly due to timeout or network issues, then you can use the--singularity_pull_docker_container
parameter to pull and convert the Docker image instead. Alternatively, you can use thenf-core download
command to download images first, before running the pipeline. Setting theNXF_SINGULARITY_CACHEDIR
orsingularity.cacheDir
Nextflow options enables you to store and re-use the images from a central location for future pipeline runs. - If you are using
conda
, it is highly recommended to use theNXF_CONDA_CACHEDIR
orconda.cacheDir
settings to store the environments in a central location for future pipeline runs.
- The pipeline comes with config profiles called
-
Start running your own analysis!
Documentation
The nf-core/mhcquant pipeline comes with documentation about the pipeline usage, parameters and output.
Credits
nf-core/mhcquant was originally written by Leon Bichmann from the Kohlbacher Lab.The pipeline was re-written in Nextflow DSL2 and is primarily maintained by Marissa Dubbelaar from Clinical Collaboration Unit Translational Immunology and Quantitative Biology Center in Tübingen.
Helpful contributors: - Lukas Heumos - Alexander Peltzer - Maxime Garcia - Gisela Gabernet - Leon Kuchenbecker - Phil Ewels - Christian Fufezan - Sven Fillinger - Kevin Menden
Contributions and Support
If you would like to contribute to this pipeline, please see the contributing guidelines.
For further information or help, don’t hesitate to get in touch on the Slack #mhcquant
channel (you can join with this invite).
Citations
If you use nf-core/mhcquant for your analysis, please cite it using the following doi: 10.5281/zenodo.1569909 and the corresponding manuscript:
MHCquant: Automated and Reproducible Data Analysis for Immunopeptidomics
Leon Bichmann, Annika Nelde, Michael Ghosh, Lukas Heumos, Christopher Mohr, Alexander Peltzer, Leon Kuchenbecker, Timo Sachsenberg, Juliane S. Walz, Stefan Stevanović, Hans-Georg Rammensee & Oliver Kohlbacher
Journal of Proteome Research 2019 18 (11), 3876-3884. doi: 10.1021/acs.jproteome.9b00313
An extensive list of references for the tools used by the pipeline can be found in the CITATIONS.md
file.
You can cite the nf-core
publication as follows:
The nf-core framework for community-curated bioinformatics pipelines.
Philip Ewels, Alexander Peltzer, Sven Fillinger, Harshil Patel, Johannes Alneberg, Andreas Wilm, Maxime Ulysse Garcia, Paolo Di Tommaso & Sven Nahnsen.
Nat Biotechnol. 2020 Feb 13. doi: 10.1038/s41587-020-0439-x.
In addition, references of tools and data used in this pipeline are as follows:
Fred2 Immunoinformatics Toolbox
Schubert B. et al, Bioinformatics 2016 Jul 1;32(13):2044-6. doi: 10.1093/bioinformatics/btw113. Epub 2016 Feb 26
Comet Search Engine
Eng J.K. et al, J Am Soc Mass Spectrom. 2015 Nov;26(11):1865-74. doi: 10.1007/s13361-015-1179-x. Epub 2015 Jun 27.
Percolator
Käll L. et al, Nat Methods 2007 Nov;4(11):923-5. doi: 10.1038/nmeth1113. Epub 2007 Oct 21.
Identification based RT Alignment
Weisser H. et al, J Proteome Res. 2013 Apr 5;12(4):1628-44. doi: 10.1021/pr300992u. Epub 2013 Feb 22.
Targeted peptide quantification
Weisser H. et al, J Proteome Res. 2017 Aug 4;16(8):2964-2974. doi: 10.1021/acs.jproteome.7b00248. Epub 2017 Jul 19.
MHC affinity prediction
O’Donnell T.J., Cell Syst. 2018 Jul 25;7(1):129-132.e4. doi: 10.1016/j.cels.2018.05.014. Epub 2018 Jun 27.
Shao X.M., Cancer Immunol Res. 2020 Mar;8(3):396-408. doi: 10.1158/2326-6066.CIR-19-0464. Epub 2019 Dec 23.