mjoppich / bioGUILinks
bioGUI provides install modules for bioinformatic software for users and allows developers to script a GUI for their applications.
☆21Updated last year
Alternatives and similar repositories for bioGUI
Users that are interested in bioGUI are comparing it to the libraries listed below
Sorting:
- Exascale Maximum Likelihood (ExaML) code for phylogenetic inference using MPI☆50Updated 5 years ago
- FAST: Fast Analysis of Sequences Toolbox☆31Updated 6 years ago
- Automatic quality control for FASTQ sequencing files☆13Updated 7 years ago
- Maximum likelihood demultiplexing☆50Updated 11 months ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆98Updated 2 years ago
- MIRROR OF: The European Molecular Biology Open Software Suite (from git://anonscm.debian.org/debian-med/emboss.git)☆29Updated 3 years ago
- Combine reference and assembled transcriptomes for RNA-Seq analysis☆23Updated 5 years ago
- Malleable All-seeing Journal Of Research Artifacts☆35Updated 2 years ago
- DEvis: an R package for aggregation and visualization of differential expression data☆19Updated 5 years ago
- Deprecated see https://github.com/MHH-RCUG/nf_wochenende : A whole Genome/Metagenome Sequencing Alignment Pipeline in Python3☆37Updated 3 years ago
- a wee tool for random access into BGZF files.☆86Updated 7 years ago
- Validate FastQ Files☆36Updated 7 years ago
- Workflow management with Nextflow and nf-core☆29Updated last year
- This repository has been archived, currently maintained version is at https://github.com/iii-companion/companion☆21Updated 4 years ago
- SeqMonk NGS visualisation and analysis tool☆51Updated 2 months ago
- The command-line interface to GGD☆43Updated 3 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 7 years ago
- Documentation of the Snakemake-Profiles project.☆55Updated 3 years ago
- adds sample names and read-group (RG) tags to BAM alignments☆51Updated 5 years ago
- A toolkit for annotation of transposable element families from unassembled sequence reads☆31Updated last month
- LoFreq Version 3☆27Updated 4 years ago
- ☆38Updated 2 months ago
- Please consider using/contributing to https://github.com/nf-core/sarek☆41Updated 4 years ago
- RetroSeq is a bioinformatics tool that searches for mobile element insertions from aligned reads in a BAM file and a library of reference…☆67Updated 3 years ago
- Useful set of classes for creating statistical genetic programs.☆52Updated 2 years ago
- ⛰ covtobed | Convert the coverage track from a BAM file into a BED file☆44Updated 3 months ago
- A collection of modules and sub-workflows for Nextflow☆28Updated 3 months ago
- An integrated high performance bioinformatics toolkit☆23Updated 6 years ago
- MPBoot: Fast phylogenetic maximum parsimony tree inference and bootstrap approximation☆20Updated last year
- detection of duplications and deletions using Python based machine learning techniques☆28Updated 6 years ago