TickingClock1992 / RIdeogramLinks
☆183Updated 5 years ago
Alternatives and similar repositories for RIdeogram
Users that are interested in RIdeogram are comparing it to the libraries listed below
Sorting:
- an R/shiny application for creation of Circos plot interactively☆157Updated 3 years ago
- Visualize and annotate genomic coverage with ggplot2☆262Updated 8 months ago
- Learning the Variant Call Format☆144Updated 2 months ago
- Match up paired end fastq files quickly and efficiently.☆152Updated last year
- Web application to explore the Sequence Read Archive.☆217Updated 2 months ago
- Visualizing transcript structure and annotation using ggplot2☆160Updated last year
- web documentation for Trinotate☆48Updated 2 years ago
- A library for running k-mers based GWAS☆116Updated 11 months ago
- Accurate and rapid RiboRNA sequences Detector based on deep learning☆115Updated last year
- Intervene: a tool for intersection and visualization of multiple genomic region and gene sets☆143Updated last year
- A pipeline to generate a phylogenetic tree from huge SNP data☆91Updated last year
- A versatile aligning pipeline for bisulfite sequencing data☆65Updated 6 years ago
- Genomic Interactive Visualization Engine☆145Updated 2 years ago
- FEELnc : FlExible Extraction of LncRNA☆90Updated 2 months ago
- LDBlockShow: a fast and convenient tool for visualizing linkage disequilibrium and haplotype blocks based on VCF files☆188Updated 3 months ago
- RNA-Seq analysis workflow☆105Updated 4 years ago
- ShortStack: Comprehensive annotation and quantification of small RNA genes☆94Updated 4 months ago
- Nanopore data analysis in R☆40Updated 2 years ago
- A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles - fo…☆106Updated 3 months ago
- 10x Genomics Linked-Read Diploid De Novo Assembler☆65Updated 6 years ago
- A set of functions to visualise genotypes based on a VCF☆87Updated 3 years ago
- Command-line tool for the visualization of splicing events across multiple samples☆130Updated last year
- csf fork of fastqc for usage on selected reads of unaligned bam file☆48Updated 12 years ago
- functions to analyse sanger sequencing reads in R☆102Updated 7 months ago
- Trinotate source code☆83Updated last year
- ☆73Updated 3 years ago
- Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project☆138Updated last month
- BAM Statistics, Feature Counting and Annotation☆150Updated last week
- Check strandedness of RNA-Seq fastq files☆125Updated 3 years ago
- A catalogue of available long read sequencing data analysis tools☆78Updated 2 weeks ago