chanjo
importedsoftware/chanjo
Chanjo provides a better way to analyze coverage data in clinical sequencing.
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- active
- Maturity
- deployed
- Organization
- Clinical-Genomics
- Country
- unknown
- Repository
- github.com/Clinical-Genomics/chanjo
- Documentation
- unknown
- Tags
- bioconda · coverage · genomics · python · sambamba · sql
- Regulatory
- unknown
Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- goleftcoverage · genomics
goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary
- seqfu2bioconda · genomics
:rocket: seqfu - Sequece Fastx Utilities
- rasusacoverage
Randomly subsample sequencing reads or alignments
- sequanacoverage
Sequana: a set of Snakemake NGS pipelines
- bioinfo-notebookbioconda
🔬 Bioinformatics Notebook. Scripts for bioinformatics pipelines, with quick start guides for programs and video demonstrations.
- MultiQCbioconda
Aggregate results from bioinformatics analyses across many samples into a single report.
- api.github.com/repos/Clinical-Genomics/chanjoretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2026-05-08, 50 stars, license reported as MIT. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/34.json→ .entries["chanjo"]
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