NCBI-Hackathons / Bringing-the-Power-of-Synthetic-Data-Generation-to-the-MassesLinks
We aim to make it easier for biomedical researchers to access and customize synthetic sequence data for the purpose of sharing and testing analysis methods as well as training and collaboration
☆11Updated 6 years ago
Alternatives and similar repositories for Bringing-the-Power-of-Synthetic-Data-Generation-to-the-Masses
Users that are interested in Bringing-the-Power-of-Synthetic-Data-Generation-to-the-Masses are comparing it to the libraries listed below
Sorting:
- ☆28Updated 6 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 6 years ago
- Haystack: Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆47Updated 3 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 8 years ago
- Machine learning use cases for teaching☆13Updated 8 years ago
- Public data resources and Bioconductor: The goal of this workshop is to introduce Bioconductor packages for finding, accessing, and using…☆14Updated 4 months ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- Machine Learning to Detect Cancer Biomarkers from RNAseq Data☆34Updated 6 years ago
- Differential Mutation Analysis☆11Updated 5 years ago
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- ☆12Updated 6 years ago
- Library for indexing VCF files for random access searches by rsID☆17Updated last month
- ☆25Updated 4 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago
- ☆17Updated last year
- ☆15Updated 2 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 6 years ago
- qtools has helper functions to submit jobs to compute clusters (PBS on TSCC, SGE on oolite) from within Python☆21Updated last year
- Boiler: a software tool for highly efficient, lossy compression of RNA-seq alignments☆13Updated 9 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- Code to reproduce analyses from the sleuth paper☆16Updated 6 years ago
- CWL implementation of CloudNeo: A cloud pipeline for identifying patient-specific tumor neoantigens☆19Updated 6 years ago
- Allele frequency filter app☆14Updated 3 years ago
- User-friendly Bioinformatics Tools☆18Updated 4 years ago
- ☆14Updated 5 years ago
- A framework for network analysis and display of SNPs☆19Updated 8 years ago
- Easily run WDL workflows on GCP☆14Updated 3 years ago