mfiers / MoaLinks
Lightweight workflows in bioinformatics:
☆24Updated 11 years ago
Alternatives and similar repositories for Moa
Users that are interested in Moa are comparing it to the libraries listed below
Sorting:
- Infrastructure code to support DNA pipeline☆38Updated 10 years ago
- A tool for running bioinformatics workflows locally or in the cloud.☆30Updated 6 years ago
- GUI for batch primer design with graphical output for PCR and SNP detection☆17Updated 7 years ago
- Toil workflows for common genomic pipelines☆33Updated 6 years ago
- Streaming algorithm for computing kmer statistics for massive genomics datasets☆54Updated 5 years ago
- Benchmarking toolkit for variant calling☆48Updated 5 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- FAstqc DAta PArser - A minimal parser to parse FastQC output data.☆16Updated 9 years ago
- A genomics pipeline build on top of the GATK Queue framework. Main repository: https://github.com/NationalGenomicsInfrastructure/piper (m…☆21Updated 9 years ago
- A web wrapper for GeneValidator☆11Updated 4 years ago
- A library for next generation genomics in Python 3☆18Updated 7 years ago
- A lightweight Python graphing API for genomic features☆15Updated 3 years ago
- An approximate sequence pattern matcher for FASTQ/FASTA files.☆31Updated 9 years ago
- Simple tokenised template system for SGE☆10Updated 2 years ago
- a simple read-only sequence database, designed for short reads☆65Updated last year
- Random collection of bioinformatics thingies☆19Updated 9 years ago
- High throughput, pain-free big data pipelines.☆30Updated 8 years ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆98Updated 2 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- ☆36Updated 8 months ago
- Inferring spatiotemporal dynamics of the H1N1 influenza pandemic from sequence data☆33Updated 12 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 6 years ago
- An integrated high performance bioinformatics toolkit☆23Updated 6 years ago
- Docker images of bioinformatics software☆21Updated 8 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 12 years ago
- ALPACA is a caller for genomic variants (single nucleotide and small indels) from next-generation sequencing data that uses a novel algeb…☆23Updated last year
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- SVG based genome viewer written in javascript using D3☆33Updated 10 years ago
- reference free variant assembly☆34Updated 2 years ago
- A python script used to annotate genomic intervals.☆18Updated 5 years ago