dapogon / cellcoal
CellCoal: coalescent simulation of single-cell NGS genotypes
☆16Updated 3 months ago
Alternatives and similar repositories for cellcoal:
Users that are interested in cellcoal are comparing it to the libraries listed below
- CellPhy: accurate and fast probabilistic inference of single-cell phylogenies☆19Updated 2 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- CHISEL -- Copy-number Haplotype Inference in Single-cell by Evolutionary Links☆38Updated 5 months ago
- ☆26Updated last month
- Multi-sample cancer phylogeny reconstruction☆35Updated 7 years ago
- Identify cell barcodes from single-cell genomics sequencing experiments☆43Updated 3 years ago
- Short Time-series Expression Miner (STEM) and Dynamic Regulatory Events Miner (DREM)☆20Updated 4 years ago
- Differential ATAC-seq toolkit☆27Updated last year
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆29Updated 9 months ago
- Create a cromphensive report of DEG list coming from any analysis of RNAseq data☆26Updated last year
- RNA-seq workflow: differential transcript usage☆21Updated last year
- interactive plots for differential expression analysis☆32Updated last month
- post-clustering differential expression test☆35Updated 5 years ago
- ☆28Updated 9 months ago
- FREE Divergence Error-Correcting DNA Barcodes☆8Updated 6 years ago
- A deme-based, spatially explicit model of intra-tumour population genetics☆21Updated 3 months ago
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆37Updated last year
- Useful tools for working with Salmon output☆37Updated 4 years ago
- R package for Enrichment Depletion Logos (EDLogos) and String Logos☆27Updated 6 years ago
- Allele-Specific Expression by Single-Cell RNA Sequencing☆28Updated 4 years ago
- Code and simulations using biologically annotated neural networks☆21Updated 3 years ago
- Support code for NGS copy number algorithms. Takes a file of locations and a [cr|b]am file and generates a count of coverage of each alle…☆44Updated 2 years ago
- Model-based subclonal deconvolution from bulk sequencing.☆33Updated 4 months ago
- ☆28Updated 5 months ago
- Create QC and summary reports for Alevin output☆32Updated 3 weeks ago
- Tools for visualizing genomics data☆68Updated 3 years ago
- Dirichlet Process based methods for subclonal reconstruction of tumours☆29Updated last month
- Code used for the single-cell RNA-Seq batch effects paper☆10Updated 7 years ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 2 months ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 2 years ago