ekfchan / evachan.org-RscriptsLinks
Handy genetics-related R scripts
☆32Updated 6 years ago
Alternatives and similar repositories for evachan.org-Rscripts
Users that are interested in evachan.org-Rscripts are comparing it to the libraries listed below
Sorting:
- Pipeline to take VCF through to Selection Analysis.☆58Updated 3 years ago
- Integrative analysis of structural variations.☆40Updated 2 years ago
- ☆30Updated 4 years ago
- Nanopore data analysis in R☆40Updated 2 years ago
- Shiny apps for teaching Population Genetics☆66Updated 2 years ago
- Evolutionary Transcriptomics with R☆47Updated last month
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 3 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- A set of R functions that help faciliate a lot of tedious processing☆18Updated 7 years ago
- QUILT: Low coverage whole genome sequence imputation with large reference panels☆65Updated last month
- ☆78Updated 11 years ago
- Adapters for trimming☆30Updated 6 years ago
- Welcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees…☆26Updated 3 years ago
- ☆17Updated 10 years ago
- Analysis of genotyping and next-generation sequencing data in medical and population genetics☆23Updated 3 years ago
- Scripts to calculate population genetics statistics☆55Updated 7 years ago
- PrimerTree: Visually Assessing the Specificity and Informativeness of Primer Pairs☆52Updated 2 months ago
- Repository of common bioinformatics scripts☆39Updated 4 years ago
- BayeScEnv is a Fst-based, genome-scan method that uses environmental variables to detect local adaptation.☆18Updated 8 years ago
- LaTeX and associated files for lecture notes used in EEB 5348 at the University of Connecticut☆36Updated 2 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 9 months ago
- ☆10Updated 5 years ago
- R package for inferring copy number from read depth☆32Updated 3 years ago
- UNDER DEVELOPMENT--- Analysis of long non-coding RNAs from RNA-seq datasets☆34Updated 9 months ago
- A guide to manipulating genotypic data across the common formats: VCF, EIGENSTRAT and PLINK (PACKEDPED) files. Includes how to convert be…☆23Updated 2 years ago
- Using kallisto for metagenomic analysis☆49Updated 8 years ago
- DensityMap is perl tool for the visualization of features density along chromosomes☆19Updated 3 years ago
- A set of workflows written in Nextflow for Genome Annotation.☆46Updated last year
- microhaplotype visualizer and analyzer☆20Updated 4 years ago
- Perform GWAS with gemma in a simple pipeline☆27Updated 8 months ago