minipileup
importedsoftware/minipileup
Simple pileup-based variant caller
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- MIT(osi)
- Status
- maintained
- Maturity
- deployed
- Organization
- unknown
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/lh3/minipileup
- Documentation
- unknown
- Tags
- bioinformatics · 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.
- BALSAMICbioinformatics · variant-calling
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
- BaseVar2bioinformatics · variant-calling
This is the official development repository for BaseVar, which call variants for large-scale ultra low-depth(<1.0x) WGS data, especially for NIPT data and ancient DNA
- Bioinformaticsbioinformatics · variant-calling
Bioinformatics N' Stuff
- CalliNGS-NFbioinformatics · variant-calling
GATK RNA-Seq Variant Calling in Nextflow
- ccsbioinformatics · variant-calling
CCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
- Clairbioinformatics · variant-calling
Clair: Exploring the limit of using deep neural network on pileup data for germline variant calling
- api.github.com/repos/lh3/minipileupretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2025-04-25, 96 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/23.json→ .entries["minipileup"]
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