rdxon
importedsoftware/rdxon
Reference-free FASTQ filter for rare germline and somatic variants
Machine-generated from the listed sources and not yet reviewed by a human.
- Category
- Software & Systems
- Subcategory
- unknown
- License
- BSD-3-Clause(osi)
- Status
- dormant
- Maturity
- deployed
- Organization
- unknown
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/tobiasrausch/rdxon
- Documentation
- unknown
- Tags
- cancer-genomics · k-mer · pan-genome · rare-disease · reference-free · sequencing · 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.
- PopPUNKk-mer
PopPUNK 👨🎤 (POPulation Partitioning Using Nucleotide Kmers)
- scDeepSortreference-free
Cell-type Annotation for Single-cell Transcriptomics using Deep Learning with a Weighted Graph Neural Network
- minigraphpan-genome
Sequence-to-graph mapper and graph generator
- Scoarypan-genome
Pan-genome wide association studies
- harpysequencing · variant-calling
Process linked-read data, from raw sequences to phased haplotypes, batteries included. Works with WGS too!
- nRexsequencing · variant-calling
nRex: Germline and somatic single-nucleotide, short indel and structural variant calling
- api.github.com/repos/tobiasrausch/rdxonretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2023-08-03, 5 stars, license reported as BSD-3-Clause. Category and schematic were assigned by keyword heuristics and are unreviewed.
Not yet verified by a human. Correct this record →
/v1/entries/12.json→ .entries["rdxon"]
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