SBMClone
importedsoftware/sbmclone
SBMClone, a method for recovering tumor clonal composition from sparse single-cell mutation data
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
- raphael-group
- Country
- unknown
- Homepage
- unknown
- Repository
- github.com/raphael-group/SBMClone
- Documentation
- unknown
- Tags
- cancer · cancer-genomics · evolution · sequencing · single-cell
- Regulatory
- unknown
Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.
- scphylo-toolscancer · evolution · single-cell
A python toolkit for single-cell tumor phylogenetic analysis
- trisicellcancer · evolution · single-cell
Scalable tumor phylogeny inference and validation from single-cell RNA or DNA data
- HGG-oncohistonescancer · cancer-genomics · single-cell
Analysis for "K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas" (Jessa et al, Nature Genetics, 2022)
- cacaocancer · cancer-genomics
Callable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
- pyGenocancer · cancer-genomics
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
- rdxoncancer-genomics · sequencing
Reference-free FASTQ filter for rare germline and somatic variants
- api.github.com/repos/raphael-group/SBMCloneretrieved 2026-08-25 · via github-api
Machine-imported from GitHub search. Last push 2021-10-13, 9 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/52.json→ .entries["sbmclone"]
Entries are sharded 64 ways by a stable hash of the id, so a consumer can find any record without an index.