IntelLabs / Open-Omics-Acceleration-FrameworkLinks
Intel lab's open sourced data science framework for accelerating digital biology
☆49Updated 2 weeks ago
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:
- ☆72Updated 2 months ago
- Bayesian enrichment estimation in R☆11Updated 2 months ago
- Tool package to perform in-silico CRISPR analysis and assessment☆34Updated 2 months ago
- Deep Learning based variant calling toolkit - https://clara-parabricks.github.io/VariantWorks/☆48Updated 4 months ago
- ☆27Updated 11 months ago
- Comparison of Adaptive Immune Receptor Repertoires☆28Updated 11 months ago
- Python package to analyze DNA methylation data☆44Updated last week
- ☆40Updated 6 months ago
- MetaLogo: a heterogeneity-aware sequence logo generator and aligner☆21Updated 2 years ago
- Project Manager for NGS data analysis☆30Updated last week
- R tool to analyse and integrate multiple -omics data☆15Updated 2 weeks ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆59Updated 10 months ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Updated 2 years ago
- A collection of useful functions for bioinformatics data analysis☆24Updated last month
- A package for designing activity-informed nucleic acid diagnostics for viruses.☆35Updated 2 years ago
- Deep learning embedding for nucleotide sequences☆19Updated 9 months ago
- Workflow management with Nextflow and nf-core☆28Updated 11 months ago
- A tool for projecting genomic alignments to transcriptomic coordinates☆37Updated last year
- The Zavolab Automated RNA-seq Pipeline☆35Updated 5 months ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated last week
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- IRIS: Isoform peptides from RNA splicing for Immunotherapy target Screening☆28Updated last year
- RNA structure probing and post-transcriptional modifications mapping high-throughput data analysis☆43Updated this week
- Parse GFF3 into Pandas dataframes☆30Updated last year
- Collection of tools to retrieve siRNA (small interfering RNA) candidate sequences targeting your gene of interest from popular siRNA desi…☆16Updated 3 years ago
- Refining the impact of genetic evidence on clinical success☆27Updated last year
- Slinker offers a succinct and complementary method to visualise RNA-Seq data through superTranscripts.☆19Updated 3 years ago
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated 2 years ago
- Examples for gget (https://github.com/pachterlab/gget).☆39Updated 4 months ago
- GOMCL: a toolkit to cluster, evaluate, and extract non-redundant associations of Gene Ontology-based functions☆22Updated 2 years ago