bernatgel / karyoploteR
karyoploteR - An R/Bioconductor package to plot arbitrary data along the genome
☆305Updated last year
Alternatives and similar repositories for karyoploteR:
Users that are interested in karyoploteR are comparing it to the libraries listed below
- A package for including transposable elements in differential enrichment analysis of sequencing datasets.☆238Updated 3 months ago
- Web application to explore the Sequence Read Archive.☆209Updated 3 weeks ago
- A collection of scripts and notes related to genomics and bioinformatics☆200Updated 2 months ago
- Miscellaneous collection of Python and R scripts for processing Iso-Seq data☆261Updated last year
- dN/dS methods to quantify selection in cancer and somatic evolution☆216Updated last year
- Visualize and annotate genomic coverage with ggplot2☆247Updated last week
- ChIP peak Annotation, Comparison and Visualization☆233Updated this week
- R package for DNA methylation analysis☆218Updated 3 weeks ago
- This Snakemake pipeline implements the GATK best-practices workflow☆245Updated last year
- an R/shiny application for creation of Circos plot interactively☆156Updated 2 years ago
- Detecting sites of genomic enrichment☆190Updated last year
- Quick mining and visualization of NGS data by integrating genomic databases☆262Updated last year
- Plot structural variant signals from many BAMs and CRAMs☆536Updated 6 months ago
- Tools to work with variant call format files☆251Updated last month
- Tool for the Quality Control of Long-Read Defined Transcriptomes☆203Updated this week
- Fast and accurate gene fusion detection from RNA-Seq data☆231Updated 2 months ago
- A short tutorial on how to use RSEM☆136Updated 4 years ago
- Genome Assembly and Annotation Service code☆206Updated last year
- Download FASTQ files from SRA or ENA repositories.☆294Updated 3 months ago
- Differential analysis of RNA-Seq☆304Updated 6 months ago
- Statistical Analysis of RNA-Seq Tools☆106Updated last year
- Light-weight Snakemake workflow for preprocessing and statistical analysis of RNA-seq data☆161Updated last month
- RNA-seq workflow using STAR and DESeq2☆333Updated 5 months ago
- classify, merge, tracking and annotation of GFF files by comparing to a reference annotation GFF☆209Updated 6 months ago
- Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae …☆210Updated 7 months ago
- Iso-Seq - Scalable De Novo Isoform Discovery from Single-Molecule PacBio Reads☆200Updated 3 months ago
- This repository contains chromosome/contig name mappings between UCSC <-> Ensembl <-> Gencode for a variety of genomes.☆237Updated 2 years ago
- ☆146Updated 2 years ago
- Application for making ENCODE Blacklists☆283Updated 3 years ago
- SUPPA: Fast quantification of splicing and differential splicing☆268Updated 7 months ago