Caleydo / vialsLinks
Vials is a Caleydo Web application for visualizing alternative splicing based on mRNAseq data.
☆13Updated 8 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 8 months ago
- Efficient handling of FASTQ files from Python☆51Updated 2 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- BigWig manpulation tools using libBigWig and htslib☆30Updated last year
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- Chromatin segmentation in R☆19Updated 8 years ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 2 months ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 6 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated last year
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- A curated list of awesome clonality and tumor heterogeneity resources☆15Updated 6 years ago
- Tools to handle reads sequenced with unique molecular identifiers (UMIs).☆30Updated 8 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- Personal diploid genome creation and coordinate conversion☆30Updated 10 months ago
- ☆26Updated 5 years ago
- 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
- create a gemini-compatible database from a VCF☆55Updated 5 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Calib clusters barcode tagged paired-end reads based on their barcode and sequence similarity.☆40Updated 2 years ago
- Fast fusion detection using kallisto☆79Updated 7 months ago
- Stupid Simple Structural Variant View☆25Updated 9 years ago
- A tool for Read Multi-Mapper Resolution☆24Updated 8 years ago
- ☆13Updated 8 years ago
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆26Updated 9 years ago
- User-friendly Bioinformatics Tools☆18Updated 4 years ago
- Fluff is a Python package that contains several scripts to produce pretty, publication-quality figures for next-generation sequencing exp…☆71Updated last year
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Updated 6 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆39Updated 4 years ago