vigsterkr / circosLinks
Circos is a software package for visualizing data and information. It visualizes data in a circular layout — this makes Circos ideal for exploring relationships between objects or positions.
☆85Updated 7 years ago
Alternatives and similar repositories for circos
Users that are interested in circos are comparing it to the libraries listed below
Sorting:
- PERF is an Exhaustive Repeat Finder☆34Updated 4 years ago
- viral-ngs: complete pipelines☆68Updated last week
- Mikado is a lightweight Python3 pipeline whose purpose is to facilitate the identification of expressed loci from RNA-Seq data * and to s…☆104Updated 9 months ago
- mtDNA Variant Caller☆35Updated 11 months ago
- Annocript is a pipeline for the annotation of de-novo generated transcriptomes. It executes BLAST analysis with UniProt, NCBI Conserved …☆56Updated 5 years ago
- De novo transcriptome assembler for short reads☆64Updated 7 years ago
- convert various features into a GFF-like file for use in genome browsers☆72Updated 4 months ago
- Interactive visualization of assembly graphs☆83Updated 3 years ago
- Highly customizable, ambiguity-aware dotplots for visual sequence analyses☆93Updated 2 weeks ago
- Dotplot large Genomes in an Interactive, Efficient and Simple way☆108Updated 2 weeks ago
- ☆32Updated 4 years ago
- simuG: a general-purpose genome simulator☆96Updated 5 months ago
- Coding Genome Reconstruction using Iso-Seq data☆62Updated 4 years ago
- Error correction for Illumina RNA-seq reads☆67Updated last year
- A snakemake pipeline for SV analysis from nanopore genome sequencing☆52Updated 5 years ago
- Lima - Demultiplex Barcoded PacBio Samples☆67Updated 6 months ago
- Simple code snippets and data for the One Flowcell - One Assembly study☆35Updated 7 years ago
- GFF3sort: A Perl Script to sort gff3 files and produce suitable results for tabix tools☆51Updated 5 years ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated last week
- Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.☆109Updated 3 years ago
- EDGE is a highly adaptable bioinformatics platform that allows laboratories to quickly analyze and interpret genomic sequence data.☆75Updated 2 months ago
- CoGe (Comparative Genomics) Platform☆46Updated 3 years ago
- VCF-kit: Assorted utilities for the variant call format☆132Updated 4 months ago
- Genome scaffolding based on HiC data in heterozygous and high ploidy genomes☆60Updated 10 months ago
- Building SuperTranscripts: A linear representation of transcriptome data☆68Updated 4 years ago
- Renders a collection of sequences into a pangenome graph. https://doi.org/10.1093/bioinformatics/btae609.☆100Updated this week
- A collection of scripts for processing fastq files in ways to improve de novo transcriptome assemblies, and for evaluating those assembli…☆51Updated last year
- A fork of exonerate: a generic tool for sequence alignment☆70Updated last year
- Transcripts annotation and GO enrichment Fisher tests☆27Updated 2 years ago
- Tools for the analysis of structural variation in genomes☆81Updated last year