AndersenLab / IBiS-Bootcamp
☆40Updated 8 years ago
Alternatives and similar repositories for IBiS-Bootcamp:
Users that are interested in IBiS-Bootcamp are comparing it to the libraries listed below
- Readshift: A method to shift high-quality NGS datasets into noisy datasetsUpdated 6 years ago
- Library for indexing VCF files for random access searches by rsID☆17Updated last year
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- A minimal copy fastq and fasta reader built for parallel support and paired end processing☆13Updated last week
- Visualization and charting JS library for streaming genomic data☆19Updated 4 months ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- ☆10Updated 7 years ago
- ☆13Updated 7 years ago
- qtools has helper functions to submit jobs to compute clusters (PBS on TSCC, SGE on oolite) from within Python☆21Updated last year
- A flexible python program for generating figures from regions of the genome.☆13Updated 6 years ago
- Docker images of bioinformatics software☆21Updated 7 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- smallgenomeutilities is a collection of Python scripts to convert alignments between different reference genomes.☆11Updated this week
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 4 months ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Ebola virus surveillance☆16Updated 8 years ago
- Align short reads against viral genomes in protein space☆10Updated 6 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- Benchmarks for RNA-seq quantification pipelines☆8Updated 5 years ago
- A fast, easy way to present complex bioinformatics pipelines to biologists☆11Updated 6 years ago
- Easily run WDL workflows on GCP☆13Updated 3 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- Color DNA/RNA bases in terminal output☆21Updated 7 years ago
- R tools to interact with hap.py output☆15Updated 5 years ago
- A swift, versatile phylogenomic and high-throughput sequencing simulator☆8Updated last year
- haplotypes genotypes and alleles example decision synthesizer☆20Updated 5 years ago
- Intro to workflows for efficient automated data analysis, using snakemake.☆32Updated 6 years ago
- Exercises for training scientists to perform some RNA-seq analyses.☆11Updated 5 years ago