Caleydo / vialsLinks
Vials is a Caleydo Web application for visualizing alternative splicing based on mRNAseq data.
☆13Updated 7 years ago
Alternatives and similar repositories for vials
Users that are interested in vials are comparing it to the libraries listed below
Sorting:
- What's The Function of these genes?☆22Updated 8 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated 3 months ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated last year
- ☆25Updated 4 years ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- User-friendly Bioinformatics Tools☆18Updated 4 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- conda recipes for genomic data☆85Updated 4 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- A curated list of awesome clonality and tumor heterogeneity resources☆15Updated 6 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- A tool for Read Multi-Mapper Resolution☆24Updated 8 years ago
- Personal diploid genome creation and coordinate conversion☆30Updated 5 months ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- MetaSRA: normalized sample-specific metadata for the Sequence Read Archive☆44Updated last month
- Fluff is a Python package that contains several scripts to produce pretty, publication-quality figures for next-generation sequencing exp…☆71Updated last year
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆71Updated 2 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- A software for the multispecies design of CRISPR/Cas9 libraries☆36Updated 2 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆52Updated 7 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆40Updated 4 years ago
- Epigenetic Variability and Transcription Factor Motifs Analysis Pipeline☆31Updated 7 years ago
- The Read Origin Protocol (ROP) is a computational protocol that aims to discover the source of all reads, including those originating fro…☆36Updated last year
- ☆20Updated 8 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆51Updated 8 months ago
- A versatile and efficient RNA-Seq read counting tool☆16Updated 9 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆39Updated 2 years ago
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago