ClairS

Category

Software & Systems

Subcategory

unknown

License

BSD-3-Clause(osi)

Status

active

Maturity

deployed

Organization

HKU-BAL

Country

unknown

Homepage

unknown

Repository

github.com/HKU-BAL/ClairS

Documentation

unknown

Tags

bioinformatics · deep-learning · genomics · haplotypes · illumina · indels · long-read-sequencing · long-reads

Regulatory

unknown

• zhengzhenxian
• JasonCLEI
• aquaskyline
• xingyaoc
• cjalder

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.

• ClairS-TObioinformatics · genomics · illumina · long-read-sequencing · long-reads

  ClairS-TO - a deep-learning method for tumor-only somatic variant calling

• octopusbioinformatics · genomics · haplotypes

  Bayesian haplotype-based mutation calling

• viralreconillumina · long-read-sequencing

  Assembly and intrahost/low-frequency variant calling for viral samples

• cievadbioinformatics · genomics · indels

  A tool suite for a simple, streamlined and rapid evaluation of variant callsets

• tiptoftbioinformatics · genomics · long-reads

  Predict plasmids from uncorrected long read data

• RUN-DVCbioinformatics · genomics · long-read-sequencing

  Generalizing deep learning-based variant callers via domain adaptation and semi-supervised learning

1. api.github.com/repos/HKU-BAL/ClairS
   retrieved 2026-08-05 · via github-api

   Machine-imported from GitHub search. Last push 2026-07-17, 112 stars, license reported as BSD-3-Clause. Category and schematic were assigned by keyword heuristics and are unreviewed.

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/v1/entries/23.json→ .entries["clairs"]

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