MutScan
importedsoftware/mutscan
Detect and visualize target mutations by scanning FastQ files directly
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- OpenGene
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/OpenGene/MutScan
- Documentation
- unknown
- Tags
- bioinformatics · cancer · detection · fastq · mutation · ngs · somatic · validation · variant · visualization
- 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.
- mgp1000bioinformatics · cancer · somatic
Nextflow bioinformatics pipeline for large-scale analysis of Multiple Myeloma genomes
- gencorebioinformatics · ngs · somatic
Generate duplex/single consensus reads to reduce sequencing noises and remove duplications
- fastq_utilsfastq · ngs · validation
Validation and manipulation of FASTQ files, scRNA-seq barcode pre-processing and UMI quantification.
- dysgubioinformatics · variant
Toolkit for calling structural variants using short or long reads
- GenomicsDBbioinformatics · variant
High performance data storage for importing, querying and transforming variants.
- zolbioinformatics · detection · visualization
zol (& fai): large-scale targeted detection and evolutionary investigation of gene clusters (i.e. BGCs, phages, etc.)
- api.github.com/repos/OpenGene/MutScanretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2022-02-10, 157 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/20.json→ .entries["mutscan"]
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