ref-solver
importedsoftware/ref-solver
Identify which human reference genome was used to align a BAM/SAM/CRAM file
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
- fulcrumgenomics
- Country
- unknown
- Repository
- github.com/fulcrumgenomics/ref-solver
- Documentation
- unknown
- Tags
- bam · bioinformatics · cram · genomics · grch37 · grch38 · hg19 · hg38 · reference-genome · rust · sam
- Regulatory
- unknown
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- cljambam · bioinformatics · cram · genomics · sam
A DNA Sequence Alignment/Map (SAM) library for Clojure
- hts-pythonbam · bioinformatics · genomics · sam
pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)
- simplesambam · bioinformatics · genomics · sam
Simple pure Python SAM parser and objects for working with SAM records
- sambambabam · bioinformatics · sam
Tools for working with SAM/BAM data
- variantkeygenomics · reference-genome
Numerical Encoding for Human Genetic Variants
- Personal-Genome-Pipelinebioinformatics · genomics · grch38
Whole genome sequencing analysis pipeline for consumer hardware. 100% local, Docker-powered, free and open source.
- api.github.com/repos/fulcrumgenomics/ref-solverretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2026-07-19, 33 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/62.json→ .entries["ref-solver"]
Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.