knausb / vcfR
Tools to work with variant call format files
☆258Updated 2 months ago
Alternatives and similar repositories for vcfR:
Users that are interested in vcfR are comparing it to the libraries listed below
- karyoploteR - An R/Bioconductor package to plot arbitrary data along the genome☆308Updated last year
- Visualize and annotate genomic coverage with ggplot2☆259Updated 3 months ago
- an R/shiny application for creation of Circos plot interactively☆157Updated 2 years ago
- adegenet: a R package for the multivariate analysis of genetic markers☆185Updated 3 months ago
- Genomic Data Retrieval with R☆221Updated 3 months ago
- Genome Association Predict Integrate Tools☆200Updated 3 weeks ago
- ChIP peak Annotation, Comparison and Visualization☆234Updated 3 weeks ago
- ☆171Updated 4 years ago
- Web application to explore the Sequence Read Archive.☆216Updated last month
- An R package for creating Q-Q and manhattan plots from GWAS results☆166Updated last year
- Publication-quality sequence logos in R☆212Updated 6 months ago
- Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis☆309Updated last year
- ➡️️➡️️⬅️️➡️️ Draw gene arrow maps in ggplot2☆540Updated last year
- Codebook from my GWAS cookbook☆190Updated 2 years ago
- Genome data visualizations☆217Updated 11 months ago
- Interface for the Basic Local Alignment Search Tool (BLAST) - R-Package☆108Updated 4 months ago
- Statistical Analysis of RNA-Seq Tools☆107Updated last month
- PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format(VCF) files☆190Updated 8 months ago
- R package for microbiome biomarker discovery☆183Updated 2 months ago
- Differential analysis of RNA-Seq☆304Updated 9 months ago
- A primer for computational tools to analyze genetics of populations in R☆86Updated 4 years ago
- Miscellaneous collection of Python and R scripts for processing Iso-Seq data☆265Updated last year
- microbiome R package☆299Updated 5 months ago
- dN/dS methods to quantify selection in cancer and somatic evolution☆222Updated last month
- Training material for introductory R / Bioconductor courses☆78Updated 2 years ago
- A package for including transposable elements in differential enrichment analysis of sequencing datasets.☆248Updated 3 months ago
- functions to analyse sanger sequencing reads in R☆101Updated 2 months ago
- This Snakemake pipeline implements the GATK best-practices workflow☆253Updated last year
- (Not Offical) BBMap short read aligner, and other bioinformatic tools.☆227Updated 4 years ago
- A simple gene co-expression analyses workflow powered by tidyverse and graph analyses☆201Updated 9 months ago