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:
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- Public data resources and Bioconductor: The goal of this workshop is to introduce Bioconductor packages for finding, accessing, and using…☆15Updated 6 months ago
- Machine learning use cases for teaching☆13Updated 8 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- ☆28Updated 7 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆29Updated last week
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- Library for indexing VCF files for random access searches by rsID☆17Updated 3 months ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 6 years ago
- Machine Learning to Detect Cancer Biomarkers from RNAseq Data☆34Updated 6 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Clonal reconstruction from HTS data☆10Updated 4 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago
- Search for activating regulatory variants in the tumor genome☆15Updated 7 months ago
- Unix-based RNA-seq quantification pipeline☆10Updated 9 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- ☆11Updated 8 years ago
- A server for maintaining high-throughput sequencing QC data☆13Updated 3 months ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 7 years ago
- A framework for network analysis and display of SNPs☆19Updated 9 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 8 years ago
- ☆26Updated 5 years ago
- Haystack: Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆47Updated 3 years ago
- mitochondrial variant analysis tools☆15Updated 4 years ago
- qtools has helper functions to submit jobs to compute clusters (PBS on TSCC, SGE on oolite) from within Python☆21Updated 2 years ago
- ☆12Updated 6 years ago
- scpca-nf is the Nextflow workflow for processing Single-cell Pediatric Cancer Atlas Portal data☆13Updated this week
- Interactive eQTL visualizations☆13Updated 2 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year