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
- Haystack: Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆47Updated 3 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago
- Machine learning use cases for teaching☆13Updated 8 years ago
- Differential Mutation Analysis☆11Updated 5 years ago
- Telomerecat: The telomere computational analysis tool☆14Updated 5 years ago
- Machine Learning to Detect Cancer Biomarkers from RNAseq Data☆34Updated 6 years ago
- Code to reproduce analyses from the sleuth paper☆16Updated 6 years ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 6 years ago
- Clonal reconstruction from HTS data☆10Updated 3 years ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15Updated 6 years 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
- ☆28Updated 7 years ago
- Public data resources and Bioconductor: The goal of this workshop is to introduce Bioconductor packages for finding, accessing, and using…☆15Updated 5 months ago
- Library for indexing VCF files for random access searches by rsID☆17Updated 2 months ago
- ☆12Updated 6 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 8 years ago
- Targeted and non-targeted anticancer drugs and drug regimens☆29Updated this week
- RNA-Seq normalization and quantification pipeline☆12Updated 10 months ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- netSmooth: A Network smoothing based method for Single Cell RNA-seq imputation☆28Updated last year
- Easily run WDL workflows on GCP☆14Updated 4 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Updated 6 years ago
- This is the BWA workflow used in the PanCancer project used to allign all the BAM files.☆11Updated 2 years ago
- ☆25Updated 5 years ago
- User-friendly Bioinformatics Tools☆18Updated 4 years ago
- AnaLysis routines for ePigenomicS data - 🏫 Bioconductor project☆16Updated 2 years ago
- This repository contains the source code of the revised version of MutPanning. MutPanning is publicly available under the BSD3-Clause ope…☆12Updated 5 years ago
- A framework for network analysis and display of SNPs☆19Updated 8 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago