smped / ngsReportsLinks
☆23Updated last month
Alternatives and similar repositories for ngsReports
Users that are interested in ngsReports are comparing it to the libraries listed below
Sorting:
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 9 months ago
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago
- Filter and prioritize fusion calls☆20Updated last year
- a Shiny/R application to view and annotate copy number variations☆28Updated 2 years ago
- Sashimi plots for RNA-seq data using detected transcripts☆29Updated 8 months ago
- DRAGEN Tumor/Normal workflow post-processing☆24Updated 2 years ago
- a set of NGS pipelines☆24Updated last week
- Population-based detection of structural variation from High-Throughput Sequencing.☆33Updated 3 years ago
- novoBreak: local assembly for breakpoint detection in cancer genomes☆25Updated 7 years ago
- DriverPower☆26Updated 10 months ago
- Relative Abundance of Transcripts: An R package for the detection of Differential Transcript isoform Usage.☆34Updated 3 years ago
- interactive plots for differential expression analysis☆34Updated 5 months ago
- A small R package to make sequencing read coverage plots in R.☆40Updated last month
- Flexible Bayesian inference of mutational signatures☆37Updated 2 years ago
- 📊 An R package of RNA-seq workflow☆15Updated 3 years ago
- Integrative analysis of structural variations.☆40Updated last year
- Bulk RNA-seq Data Processing, Quality Control, and Downstream Analysis Pipeline☆20Updated 11 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Code for differential splicing comparison paper (Soneson, Matthes, et al.)☆20Updated 9 years ago
- A series of scripts to automate sequence workflows☆19Updated 6 months ago
- Make rapid visualizations of RNA-seq data in R☆19Updated 2 months ago
- AnaLysis routines for ePigenomicS data - 🏫 Bioconductor project☆16Updated 2 years ago
- ☆21Updated last year
- Interactive R package to quantify, analyse and visualise alternative splicing☆37Updated last week
- Calculate and plot distributions of genomic ranges☆26Updated 7 months ago
- RNA-seq analysis scripts☆15Updated last month
- RNA-seq for Mendelian disease diagnostics: A hands-on tutorial through bioinformatic tools and workflows☆17Updated 3 years ago
- Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.☆36Updated last year
- An R Package based on JavaScript libraries for Visualization of Interactive Circos Plot☆28Updated 3 years ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 8 months ago