IntelLabs / Open-Omics-Acceleration-FrameworkLinks
Intel lab's open sourced data science framework for accelerating digital biology
☆49Updated this week
Alternatives and similar repositories for Open-Omics-Acceleration-Framework
Users that are interested in Open-Omics-Acceleration-Framework are comparing it to the libraries listed below
Sorting:
- Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/☆47Updated last month
- Python package to analyze DNA methylation data☆43Updated 10 months ago
- ☆67Updated 6 months ago
- Parse GFF3 into Pandas dataframes☆30Updated last year
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 7 months ago
- Deep learning embedding for nucleotide sequences☆19Updated 5 months ago
- Project Manager for NGS data analysis☆31Updated 3 years ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆54Updated 6 months ago
- Bayesian enrichment estimation in R☆11Updated 3 years ago
- A package for designing activity-informed nucleic acid diagnostics for viruses.☆33Updated 2 years ago
- ☆39Updated 2 months ago
- ClinVar Mapping and Annotation Toolkit☆20Updated last week
- Workflow management with Nextflow and nf-core☆25Updated 8 months ago
- ☆76Updated 2 months ago
- A tool for projecting genomic alignments to transcriptomic coordinates☆36Updated last year
- Tool package to perform in-silico CRISPR analysis and assessment☆31Updated last year
- ☆27Updated 7 months ago
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆61Updated last week
- ☆25Updated 4 years ago
- ☆82Updated 2 weeks ago
- Interactive multiscale visualization for structural variation in human genomes☆70Updated 2 weeks ago
- MetaLogo: a heterogeneity-aware sequence logo generator and aligner☆21Updated 2 years ago
- Comparison of Adaptive Immune Receptor Repertoires☆28Updated 7 months ago
- ☆19Updated 2 years ago
- visual analysis of your VCF files☆36Updated 2 years ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Updated 2 years ago
- G4Hunter (2012_2015)- IECB - Bordeaux☆16Updated 5 years ago
- ☆10Updated 5 years ago
- EditR: an algorithm for simple and cost effective measurement of base editing by quantifying Sanger trace fluorescence☆32Updated 2 years ago
- RNA structure probing and post-transcriptional modifications mapping high-throughput data analysis☆40Updated last week