MonashBioinformaticsPlatform / learning-resource-links
An awesome list of learning resources for bioinformatics, genomics and computational biology
☆13Updated 4 months ago
Alternatives and similar repositories for learning-resource-links:
Users that are interested in learning-resource-links are comparing it to the libraries listed below
- Chromatin ACcessibility and Transcriptomics Unifying Software☆16Updated 4 months ago
- Filter and prioritize fusion calls☆20Updated 5 months ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- R package specialized in HLA typing clustering and visualization based on specific similarity metrics☆12Updated 5 years ago
- ☆18Updated 7 months ago
- Interactive eQTL visualizations☆13Updated 2 years ago
- DRAGEN Tumor/Normal workflow post-processing☆22Updated last year
- RNA-seq data comprehensive data analysis toolbox☆19Updated 2 years ago
- software for analysis of chromatin feature occupancy profiles from high-throughput sequencing data☆16Updated 5 years ago
- Winter 2021, GGG 298 - Tools for Data Intensive Research - UC Davis☆13Updated 3 years ago
- ☆21Updated 9 months ago
- Python function for TMB snake plots☆16Updated 4 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago
- NHC: A computational approach to detect physiological homogeneity in the midst of genetic heterogeneity☆10Updated last year
- interactive plots for differential expression analysis☆31Updated this week
- Machine learning use cases for teaching☆13Updated 7 years ago
- a Shiny/R application to view and annotate copy number variations☆28Updated last year
- 📊 An R package of RNA-seq workflow☆16Updated 2 years ago
- ☆10Updated 5 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆26Updated 6 years ago
- a set of NGS pipelines☆24Updated this week
- Predicting TF sequence-specificity similarity with weighted alignments☆13Updated 5 years ago
- mitochondrial variant analysis tools☆14Updated 3 years ago
- A small R package to make sequencing read coverage plots in R.☆37Updated 2 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 3 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 5 months ago
- A command line tool to compute mapping statistics from a BAM file☆23Updated 2 years ago
- Pipelines for NGS data preprocessing by the Bock lab and friends☆20Updated 2 years ago
- Differential Hi-C Data Analysis Workshop https://currentprotocols.onlinelibrary.wiley.com/doi/abs/10.1002/cpbi.76☆15Updated 3 years ago
- Reconstructs complex variation using Bionano optical mapping data and breakpoint graph data☆16Updated last year