UMIseq_variant_calling
importedsoftware/umiseq-variant-calling
Detect somatic SNVs from deep targeted UMI-seq cfDNA
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
- BesenbacherLab
- Country
- unknown
- Homepage
- unknown
- Documentation
- unknown
- Tags
- cell-free · umi-seq · 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.
- arcsvvariant-calling
Complex structural variant detection from WGS data
- BALSAMICvariant-calling
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
- bam-to-ychr-callsvariant-calling
From .bam to .csv with annotated Y-chromosome variants
- BaseVar2variant-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
- BaseVarCvariant-calling
The repo was not under active development. Check out angsd toolkit for low depth data analyses.
- Bioinformaticsvariant-calling
Bioinformatics N' Stuff
- api.github.com/repos/BesenbacherLab/UMIseq_variant_callingretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2026-01-27, 3 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/16.json→ .entries["umiseq-variant-calling"]
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