BALSAMIC
importedsoftware/balsamic
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
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
- Homepage
- balsamic.readthedocs.io/
- Repository
- github.com/Clinical-Genomics/BALSAMIC
- Documentation
- unknown
- Tags
- bioinformatics · genomics · snakemake-workflows · somatic-mutations · variant-calling
- 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.
- nRexsomatic-mutations · variant-calling
nRex: Germline and somatic single-nucleotide, short indel and structural variant calling
- CalliNGS-NFbioinformatics · genomics · variant-calling
GATK RNA-Seq Variant Calling in Nextflow
- dysgubioinformatics · genomics · variant-calling
Toolkit for calling structural variants using short or long reads
- NCHHSTP-DTBE-Varpipe-WGSbioinformatics · genomics · variant-calling
This repository contains an analysis pipeline developed to characterize WGS output
- nf-ncov-vocbioinformatics · genomics · variant-calling
A Nextflow wrapped workflow for generating the mutation profiles of SARS-CoV-2 or Mpox genomes. Workflow is developed in collaboration with VIRUS-MVP (https://github.com/cidgoh/VIRUS-MVP) which can…
- octopusbioinformatics · genomics · variant-calling
Bayesian haplotype-based mutation calling
- api.github.com/repos/Clinical-Genomics/BALSAMICretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-07-14, 60 stars, license reported as MIT. Category and schematic were assigned by keyword heuristics and are unreviewed.
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