TiedemannLab / sciCNV
Dissecting the effects of DNA copy number variations on transcriptional programs at single-cell resolution
☆13Updated 3 years ago
Alternatives and similar repositories for sciCNV
Users that are interested in sciCNV are comparing it to the libraries listed below
Sorting:
- This repository contains scripts to identify healthy and malignant cells from scRNAseq with CloneTracer and process data from Optimized 1…☆26Updated 7 months ago
- Functions for single cell data analysis☆31Updated 3 years ago
- R package for decontaminating the spot swapping effect and recovering true expression in spatial transcriptomics data☆33Updated 11 months ago
- mutation(barcode) caller for 10x single cell data☆45Updated 4 years ago
- Single cell RNA-seq analysis bundle☆34Updated 5 years ago
- Aligning gene expression trajectories of single-cell reference and query systems☆64Updated 7 months ago
- MultiK is a data-driven tool that objectively assesses the optimal number(s) of clusters based on the concept of consensus clustering via…☆22Updated last year
- Infer Copy Number Alterations and Clonality in (Single-Cell) RNA-Seq Data☆36Updated last year
- sEV-containing droplet identification in scRNA-seq data (SEVtras)☆25Updated 2 months ago
- Inference of cell-cell communication from single-cell RNAseq data☆48Updated 3 weeks ago
- ☆20Updated last year
- MERCI for tracing of mitochondrion transfer between single cancer and T cells☆22Updated last year
- Trajectory inference across multiple conditions with condiments: differential topology, progression, differentiation, and expression☆28Updated 5 months ago
- ☆12Updated 4 years ago
- Scripts and notebooks to reproduce all analysis from Massoni-Badosa et al. (2022)☆28Updated 4 months ago
- Draw phylogenetic trees of tumor evolution☆78Updated last year
- code for data processing and visualisation associated with the stromal subclasses manuscript☆11Updated 4 years ago
- scWGCNA☆60Updated 2 years ago
- Repository to reproduce all analyses for Lareau*, Ludwig*, et al. 2020☆16Updated last year
- ☆33Updated last year
- This repository contains the CellTag data analysis R package to support clone calling and lineage reconstruction.☆21Updated 2 years ago
- Method for de novo mutation calling from droplet based single cell RNA seq data☆14Updated 3 years ago
- ☆13Updated last year
- ☆47Updated 5 years ago
- SCDC☆45Updated last year
- Repository for the building, sharing and editing of scRNAseq pipelines for the Lung Cell Atlas☆36Updated 4 years ago
- An R shiny based tool used for single cell RNA-seq data visualization and analysis.☆33Updated 4 years ago
- A tool for removing doublets from single-cell RNA-seq data☆74Updated 4 years ago
- ☆32Updated 5 years ago
- Code repository for single cell RNA-seq☆34Updated 4 years ago