https://github.com/cbg-ethz/longsom

LongSom tool for long-reads

https://github.com/cbg-ethz/longsom

Science Score: 57.0%

This score indicates how likely this project is to be science-related based on various indicators:

  • CITATION.cff file
  • codemeta.json file
    Found codemeta.json file
  • .zenodo.json file
    Found .zenodo.json file
  • DOI references
    Found 3 DOI reference(s) in README
  • Academic publication links
    Links to: biorxiv.org, nature.com
  • Committers with academic emails
  • Institutional organization owner
    Organization cbg-ethz has institutional domain (www.bsse.ethz.ch)
  • JOSS paper metadata
  • Scientific vocabulary similarity
    Low similarity (5.9%) to scientific vocabulary
Last synced: 7 months ago · JSON representation

Repository

LongSom tool for long-reads

Basic Info
  • Host: GitHub
  • Owner: cbg-ethz
  • Language: Python
  • Default Branch: main
  • Size: 274 MB
Statistics
  • Stars: 10
  • Watchers: 4
  • Forks: 1
  • Open Issues: 4
  • Releases: 2
Created about 2 years ago · Last pushed 11 months ago
Metadata Files
Readme

README.md

LongSom

A Snakemake workflow for calling somatic SNVs, fusions, and CNAs in high-quality long-read single-cell RNA-seq cancer samples, and infer subclonal structures based on those variants.

LongSom takes a bam file and a barcodes file as input. Before calling variants, it performs a cell types reannotation step for improved results. For more informations about the methods, please read our Genome Research publication Dondi et al. 2025.

For more information, including installation and usage, please visit our Wiki.

Workflow

Flowchart

Cite

If you use LongSom, please cite:

Arthur Dondi, Nico Borgsmüller, Pedro Ferreira, Brian Haas, Francis Jacob, Viola Heinzelmann-Schwarz, Tumor Profiler Consortium, Niko Beerenwinkel. De novo detection of somatic variants in high-quality long-read single-cell RNA sequencing data. Genome Research (2025)

In addition, please cite SComatic if you use LongSom for SNV detection, CTAT-LR-fusion for fusion detection, and BnpC for subclonal structure reconstruction.

Owner

  • Name: Computational Biology Group (CBG)
  • Login: cbg-ethz
  • Kind: organization
  • Location: Basel, Switzerland

Beerenwinkel Lab at ETH Zurich

GitHub Events

Total
  • Issues event: 8
  • Watch event: 6
  • Issue comment event: 1
  • Push event: 2
  • Pull request event: 1
  • Gollum event: 5
  • Fork event: 1
Last Year
  • Issues event: 8
  • Watch event: 6
  • Issue comment event: 1
  • Push event: 2
  • Pull request event: 1
  • Gollum event: 5
  • Fork event: 1

Committers

Last synced: 10 months ago

All Time
  • Total Commits: 14
  • Total Committers: 1
  • Avg Commits per committer: 14.0
  • Development Distribution Score (DDS): 0.0
Past Year
  • Commits: 13
  • Committers: 1
  • Avg Commits per committer: 13.0
  • Development Distribution Score (DDS): 0.0
Top Committers
Name Email Commits
ArthurDondi a****i@g****m 14

Issues and Pull Requests

Last synced: 10 months ago

All Time
  • Total issues: 2
  • Total pull requests: 1
  • Average time to close issues: N/A
  • Average time to close pull requests: N/A
  • Total issue authors: 1
  • Total pull request authors: 1
  • Average comments per issue: 1.5
  • Average comments per pull request: 0.0
  • Merged pull requests: 0
  • Bot issues: 0
  • Bot pull requests: 0
Past Year
  • Issues: 2
  • Pull requests: 1
  • Average time to close issues: N/A
  • Average time to close pull requests: N/A
  • Issue authors: 1
  • Pull request authors: 1
  • Average comments per issue: 1.5
  • Average comments per pull request: 0.0
  • Merged pull requests: 0
  • Bot issues: 0
  • Bot pull requests: 0
Top Authors
Issue Authors
  • HarrisonWismer (2)
  • hwismer (2)
  • modalaigh (1)
  • xuxif (1)
Pull Request Authors
  • rezabehboudi (2)
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