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 5 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:
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- Distinguishing between generic and experiment-specific gene expression signals.☆12Updated 2 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Updated 6 years ago
- Clonal reconstruction from HTS data☆10Updated 3 years ago
- Machine learning use cases for teaching☆13Updated 7 years ago
- Library for indexing VCF files for random access searches by rsID☆17Updated last year
- iDEP: integrated Differential Expression & Pathway analysis☆15Updated 6 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- ☆11Updated 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
- Collection of scripts for pre- and postprocessing neoantigen discovery calls.☆9Updated 5 years ago
- Building the constrained coding regions (CCR) model☆16Updated 6 years ago
- PharmGKB NGS Pipeline☆17Updated 6 years ago
- The OpEx (Optimised Exome) pipeline☆9Updated 6 years ago
- Public data resources and Bioconductor: The goal of this workshop is to introduce Bioconductor packages for finding, accessing, and using…☆14Updated 3 weeks ago
- robust matching of small variant datasets using flexible scoring schemes☆10Updated 5 years ago
- Allele-Specific Quantification of Structural Variations in Cancer Genomes☆17Updated 6 years ago
- Gene expression viewer template☆11Updated 7 years ago
- The vignette provided has a basic sketch of the steps we interactively will go through to build a package with devtools, explains version…☆11Updated 4 years ago
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆13Updated 3 years ago
- Allele frequency filter app☆14Updated 3 years ago
- Convert VCF (Variant Call Format) into TCGA MAF (Mutation Annotation Format)☆14Updated 8 years ago
- WES HLA Typing based on multiple alternative tools☆16Updated 4 years ago
- Easily run WDL workflows on GCP☆13Updated 3 years ago
- R tools to interact with hap.py output☆15Updated 5 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆28Updated this week
- ☆12Updated 6 years ago
- GenoTypes Compressor☆15Updated 3 years ago