Clonal and subclonal Copy Number Alteration quality check integrating somatic mutation
-
Updated
May 26, 2025 - R
#
copy-number-variations
Here are 8 public repositories matching this topic...
Total copy number inference from single-cell RNA and ATAC sequing with cell clustering
-
Updated
Oct 31, 2024 - R
Bayesian inference of gene mutant dosage from targeted panels without matched normal
-
Updated
Sep 4, 2025 - R
The Soybean Genomic Variations Explorer (Soybean GenVarX) is a toolset that consists of promoter region component and CNV component for users to perform queries, visualize data, and conduct annotations using genotypic and phenotypic differences.
transcription-factors snps promoters phenotypes indels soybean genomic-variations whole-genome-resequencing-data copy-number-variations
-
Updated
Feb 17, 2025 - PHP
Tumour evolution bioinformatics analysis pipeline from bulk sequencing
-
Updated
Aug 20, 2025
Pseudo-timing copy number alterations in cancer
-
Updated
Sep 2, 2025 - R
Genetic alterations and expression of genes coding for FGF ligands and FGF reseptors in urothelial cancer
machine-learning mutations network-analysis jaccard-similarity differential-gene-expression bladder-cancer fgf latent-class-analysis copy-number-variations multi-dimensional-scaling fgfr urothelial-cancer
-
Updated
Jun 5, 2025 - TeX
The Genomic Variations Explorer (GenVarX) is a toolset that consists of promoter region component and CNV component for users to perform queries, visualize data, and conduct annotations using genotypic and phenotypic differences.
transcription-factors snps promoters phenotypes indels soybean genomic-variations whole-genome-resequencing-data copy-number-variations
-
Updated
Jun 15, 2025 - Blade
Improve this page
Add a description, image, and links to the copy-number-variations topic page so that developers can more easily learn about it.
Add this topic to your repo
To associate your repository with the copy-number-variations topic, visit your repo's landing page and select "manage topics."