celiamtnez / snRNA-seq2_youngLinks
Analysis of snRNA-seq2 data coming from 3 months old mouse liver, dissecting the influence ploidy has on gene expression.
☆12Updated 3 years ago
Alternatives and similar repositories for snRNA-seq2_young
Users that are interested in snRNA-seq2_young are comparing it to the libraries listed below
Sorting:
- ☆23Updated 2 years ago
- ☆12Updated 4 years ago
- Matrix factorization model for interpreting single cell gene expression in biologically heterogeneous data☆21Updated last year
- ☆12Updated 5 years ago
- This is the repository which contains the code that was used to generate the results and figures of the “Single-cell RNA-sequencing revea…☆11Updated 11 months ago
- Gene Expression Decomposition and Integration☆17Updated 3 months ago
- Computational identification of targets for CAR-T cell therapy in AML☆16Updated 2 years ago
- ☆20Updated last year
- ☆20Updated last year
- ☆17Updated 2 years ago
- MOJITOO: a fast and universal method for integration of multimodal single cell data☆10Updated 7 months ago
- Code to reproduce analyses in Nasser, Bergman, Fulco, Guckelberger, Doughty et al Nature 2021☆15Updated 4 years ago
- ☆10Updated 2 years ago
- CellWalkR: An R Package for integrating single-cell and bulk data to resolve regulatory elements☆15Updated last week
- Immune Cell Gene Signatures for Profiling the Microenvironment of Solid Tumours☆27Updated 4 years ago
- Pipeline to analyze long-read mRNA isoforms and ORF products sequenced in breast cancer using PacBio Single-Molecule technology.☆15Updated 3 years ago
- ☆10Updated 4 months ago
- ☆19Updated last year
- Example of run CytoSig and reproduce prediction results on bulk and single-cell cohorts☆12Updated last year
- Analyzing chromatin accessibility data in R☆18Updated last year
- ☆17Updated 10 months ago
- A collection of perl scripts for NGS analysis☆16Updated 8 months ago
- Reproducibility code for the manuscript: 'Inferring and perturbing cell fate regulomes in human cerebral organoids☆28Updated last year
- ☆16Updated 2 years ago
- bioinformatics R test code☆14Updated this week
- In this study, we perform systematic comparative analysis of seven widely-used SNV-calling methods, including SAMtools, the GATK Best Pra…☆15Updated 5 years ago
- ☆10Updated 3 years ago
- Detecting cancer subtypes with machine learning.☆10Updated 5 years ago
- Testing a neutral evolution model on cancer sequencing data☆10Updated 4 years ago
- Code associated with MIX-seq manuscript☆15Updated 4 years ago