dcjones / poleeLinks
Analyzing RNA-Seq with approximate likelihood
☆26Updated 5 years ago
Alternatives and similar repositories for polee
Users that are interested in polee are comparing it to the libraries listed below
Sorting:
- OpenMendel package for haplotyping and imputation☆25Updated 4 months ago
- A Julia package for handle genome graph in the GFA format.☆11Updated 3 years ago
- simulate sequence data and complicated pedigree structures☆15Updated 2 years ago
- The main website for the OpenMendel project.☆13Updated 3 years ago
- BGZF Stream☆13Updated 2 years ago
- Read and write VCF and BCF files☆14Updated 3 months ago
- Quantitative Trait Cluster Association Test in R☆26Updated 4 years ago
- Julia module to handle PLINK BED files☆11Updated 7 years ago
- Fast and scalable cell search tool☆44Updated 6 years ago
- 🧬High-performance genetics- and genomics-related data visualization using Makie.jl☆89Updated 4 months ago
- ☆16Updated last year
- For analysis of microbiome and microbial community data☆47Updated 2 years ago
- Parse and process SAM and BAM formatted files☆29Updated 9 months ago
- Build and maintain multiple custom conda environments all in one place.☆40Updated last year
- 🧫 Read Flow Cytometry Standard (FCS) files in Julia☆17Updated 3 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- ☆21Updated last month
- Python-interface C++ library for Bayesian phylogenetics via optimization☆40Updated last year
- ☆17Updated last year
- Hera-T, a fast and accurate tool for estimating gene abundances in single cell data generated by the 10X-Chromium protocol☆18Updated 4 years ago
- BUS format specification☆13Updated 6 years ago
- provides common tools and lookup tables used primarily by the hgvs and uta packages☆24Updated 3 weeks ago
- Polygenic score calculation from VCF in Nim.☆15Updated 5 years ago
- Phylogenetic inference using Stan☆23Updated 11 months ago
- Stupid Simple Elastic Compute Cloud☆16Updated 2 years ago
- A flexible tool for the multi-resolution localization of causal variants across the genome☆11Updated 4 years ago
- Pipeline to produce consensus reads using unique molecular indexes/barcodes (UMIs)☆26Updated 2 months ago
- Cookiecutter profile for making a NextFlow-based bioinformatics tool☆17Updated last year
- Causal Variant Evidence Mapping with Non-parametric resampling☆12Updated 5 years ago
- Calculate indel trajectory likelihoods using methods of Miklós, Lunter & Holmes (2004), De Maio (2020), and Holmes (2020)☆14Updated 3 years ago