Reads2Map
importedsoftware/reads2map
A collection of WDL bioinformatic workflows to benchmark markers coming from different pipelines using linkage map quality as a diagnosis.
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/Cristianetaniguti/Reads2Map
- Documentation
- unknown
- Tags
- genotyping-by-sequencing · haplotypes · linkage-mapping · pipelines · variant-calling · wdl
- 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.
- long-read-pipelinespipelines · variant-calling · wdl
Long read production pipelines
- octopushaplotypes · variant-calling
Bayesian haplotype-based mutation calling
- NeuroPGxgenotyping-by-sequencing
A clinical decision-support system to identify pharmacogenomics profiles based on subjects genotype of five core genes. The paper has been published in the Journal of Personalized Medicine.
- ClairShaplotypes
ClairS: a deep-learning method for long-read tumor–normal pair somatic small variant calling
- wdlwdl
Specification for the Workflow Description Language (WDL).
- arcsvvariant-calling
Complex structural variant detection from WGS data
- api.github.com/repos/Cristianetaniguti/Reads2Mapretrieved 2026-08-05 · via github-api
Machine-imported from GitHub search. Last push 2025-09-24, 11 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/6.json→ .entries["reads2map"]
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