ChristophH / InferelatorLinks
The official Inferelator repository maintained by current or former Bonneau lab members
☆9Updated 8 years ago
Alternatives and similar repositories for Inferelator
Users that are interested in Inferelator are comparing it to the libraries listed below
Sorting:
- Mean Alterations Using Discrete Expression☆14Updated last year
- Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R☆30Updated 9 months ago
- Examples of kallisto + sleuth☆11Updated 8 years ago
- Workflow for ZINB-WaVE + DESeq2 intergration for single-cell RNA-seq☆31Updated 4 years ago
- ☆19Updated 8 years ago
- stageR package☆13Updated 2 years ago
- An R package to increase interpretability of genes and SNPs (eg identified from GWAS and eQTL mapping)☆10Updated 2 years ago
- Code for EpiMap data browser☆14Updated last year
- NHC: A computational approach to detect physiological homogeneity in the midst of genetic heterogeneity☆10Updated last year
- polygenic scores using variational inference on GWAS summary statistics from multiple cohorts☆11Updated 2 years ago
- Code and simulations using biologically annotated neural networks☆21Updated 3 years ago
- GWAS gold standards repository☆37Updated last year
- V'DJer - B Cell Receptor Repertoire Reconstruction from short read mRNA-Seq data☆29Updated 2 years ago
- A Julia package for extracting mutation signatures using topic models☆19Updated 3 years ago
- Sample code for ldsc analyses in UKBB☆31Updated 2 years ago
- Comprehensive Human Expressed SequenceS☆17Updated this week
- Learn tissue-specificity and tissue-sharing of genetic regulation across 49 tissues using constraint matrix factorization model☆22Updated 4 years ago
- ☆15Updated 6 years ago
- Summary statistics for repertoires☆17Updated 2 years ago
- Tutorial for the analysis of scRNA-seq data in R☆18Updated 6 years ago
- R/BioC package to estimate the cell composition of whole blood in DNA methylation samples in microarray or sequencing platforms☆19Updated 2 years ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆29Updated 11 months ago
- Code for reproducing results from the paper "Modular and efficient pre-processing of single-cell RNA-seq data"☆23Updated 4 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- gkmSVM R package☆17Updated 7 years ago
- Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneit…☆37Updated last year
- Repository for signature genes from Immune Cell Atlas☆18Updated 5 years ago
- A simple, intuitive and Efficient single cell binary Data Storage format☆15Updated 5 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- R package for 'Bayesian multivariate analysis of summary statistics' (Stephens Lab)☆10Updated 4 years ago