Chanjo is coverage analysis for clinical sequencing. It's implemented in Python with a command line interface that adheres to UNIX pipeline philisophy.
Chanjo is distruibuted through "pip". Install the latest release by running:
$ pip install chanjo... or locally for development:
$ git clone https://github.com/robinandeer/chanjo.git && cd chanjo
$ pip install --editable .Do note that Chanjo is built on some of kind-of tricky dependencies. If you are experiencing any issues, help is just a click away in the documentation.
Chanjo exposes a composable command line interface. You can always save intermediary files at any stage and customize every option. However, using a chanjo.toml config and UNIX pipes you can end up with something like:
$ chanjo convert CCDS.sorted.txt | chanjo annotate alignment.bam > coverage.bedRead the Docs is hosting the official documentation.
I can specifically recommend the fully interactive demo, complete with sample data to get you started right away.
If you are looking to learn more about handling sequence coverage data in clinical sequencing, feel free to download and skim through my own Master's thesis and article references.
Chanjo works on BAM alignment files and extracts interesting coverage related statistics. You use a BED-file to define which regions of the genome that you particularly care about. The output takes the shape of an extended BED-file.
An optional final step is to load data into a SQL database. This will aggregate data from exons to transcripts and genes. The database will later work as an API to downstream tools like the Chanjo Coverage Report generator.
Chanjo is not the right choice if you care about coverage for every base across the entire genome. Detailed histograms is something BEDTools already handles with confidence.
MIT. See the LICENSE file for more details.
Anyone can help make this project better - read CONTRIBUTION to get started!