nf-core/imcyto
Image Mass Cytometry analysis pipeline
22.10.6
.
Learn more.
Introduction
nfcore/imcyto is a bioinformatics analysis pipeline used for image segmentation and extraction of single cell expression data. This pipeline was generated for Imaging Mass Cytometry data, however, it is flexible enough to be applicable to other types of imaging data e.g. immunofluorescence/immunohistochemistry data.
The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It comes with docker containers making installation trivial and results highly reproducible.
Pipeline summary
-
Split image acquisition output files (
mcd
,ome.tiff
ortxt
) by ROI and convert to individualtiff
files for channels with names matching those defined in user-providedmetadata.csv
file. Full and ilastik stacks will be generated separately for all channels being analysed in single cell expression analysis, and for channels being used to generate the cell mask, respectively (imctools). -
Apply pre-processing filters to full stack
tiff
files (CellProfiler). -
Use selected
tiff
files in ilastik stack to generate a composite RGB image representative of the plasma membranes and nuclei of all cells (CellProfiler). -
Use composite cell map to apply pixel classification for membranes, nuclei or background, and save probabilities map as
tiff
(Ilastik). If CellProfiler modules alone are deemed sufficient to achieve a reliable segmentation mask this step can be bypassed using the--skip_ilastik
parameter in which case the compositetiff
generated in step 3 will be used in subsequent steps instead. -
Use probability/composite
tiff
and pre-processed full stacktiff
for segmentation to generate a single cell mask astiff
, and subsequently overlay cell mask onto full stacktiff
to generate single cell expression data incsv
file (CellProfiler).
Quick Start
i. Install nextflow
ii. Install one of docker
or singularity
iii. Download the pipeline and test it on a minimal dataset with a single command
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.
iv. Start running your own analysis!
See usage docs for all of the available options when running the pipeline.
Documentation
The nf-core/imcyto pipeline comes with documentation about the pipeline, found in the docs/
directory:
- Installation
- Pipeline configuration
- Running the pipeline
- Output and how to interpret the results
- Troubleshooting
Credits
The pipeline was originally written by The Bioinformatics & Biostatistics Group for use at The Francis Crick Institute, London.
The pipeline was developed by Harshil Patel and Nourdine Bah in collaboration with Karishma Valand, Febe van Maldegem, Emma Colliver and Mihaela Angelova.
Many thanks to others who contributed as a result of the Crick Data Challenge (Jan 2019) - Gavin Kelly, Becky Saunders, Katey Enfield, Alix Lemarois, Nuria Folguera Blasco, Andre Altmann.
It would not have been possible to develop this pipeline without the guidelines, scripts and plugins provided by the Bodenmiller Lab. Thank you too!
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 Slack (you can join with this invite).
Citation
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.
ReadCube: Full Access Link
An extensive list of references for the tools used by the pipeline can be found in the CITATIONS.md
file.