dwgoon / nezzle
Network Visualization using both GUI and Programming
☆28Updated 9 months ago
Alternatives and similar repositories for nezzle:
Users that are interested in nezzle are comparing it to the libraries listed below
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆39Updated 2 years ago
- Feature-rich Python implementation of the tximport package for gene count estimation.☆35Updated 3 weeks ago
- Benchmarking long-read RNA-seq analysis tools☆26Updated last month
- RNA-seq data comprehensive data analysis toolbox☆19Updated 2 years ago
- Accurate estimation and robust modelling of translation dynamics at codon resolution☆20Updated 7 years ago
- Versatile FASTA/FASTQ demultiplexer.☆33Updated 9 months ago
- interactive plots for differential expression analysis☆32Updated last month
- Genomic data interpretation and visualization Workshop☆19Updated last year
- Tool package to perform in-silico CRISPR analysis and assessment☆24Updated 10 months ago
- Differential ATAC-seq toolkit☆27Updated last year
- SCASA: Single cell transcript quantification tool☆20Updated last year
- ☆15Updated 2 years ago
- Millefy: Genome browser-like visualization of single-cell RNA-seq dataset☆28Updated 5 years ago
- R Shiny application for cross omics data analysis. In revision with Bioinformatics Adv.☆24Updated this week
- Accompanying analysis code for the FRASER manuscript☆26Updated 4 years ago
- Toolkit for benchmarking fusion transcript predictions☆18Updated 7 months ago
- ☆19Updated 3 months ago
- An R package to process and analyze transcriptomic data☆16Updated 6 months ago
- Comprehensive and scalable differential splicing analyses☆15Updated 2 weeks ago
- Explore the cancer relevance of your gene list☆50Updated 3 weeks ago
- ImReP is a computational method for rapid and accurate profiling of the adaptive immune repertoire from regular RNA-Seq data.☆28Updated 5 years ago
- ChIP-seq DC and QC Pipeline☆34Updated 4 years ago
- Motif manipulation functions for R.☆28Updated 4 months ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆26Updated last year
- ☆20Updated 5 years ago
- epigenome analysis to rank transcription factors☆13Updated 5 years ago
- Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.☆28Updated 4 years ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆22Updated 2 months ago
- iread☆24Updated 3 years ago
- A template repository for Snakemake pipepline(s) and a python command-line toolkit.☆28Updated last week