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:
- BigWig manpulation tools using libBigWig and htslib☆30Updated last year
- What's The Function of these genes?☆22Updated 8 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 6 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated 8 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- Expectation-Maximization algorithm for Allele-Specific Expression☆21Updated 2 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated last year
- Peakzilla is a self-learning algorithm to identify transcription factor binding sites from ChIP-seq data. I would be very happy if you tr…☆21Updated 5 months 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
- Personal diploid genome creation and coordinate conversion☆30Updated 9 months ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- A tool for Read Multi-Mapper Resolution☆24Updated 8 years ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- a wee tool for random access into BGZF files.☆86Updated 7 years ago
- Tools to handle reads sequenced with unique molecular identifiers (UMIs).☆30Updated 8 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- simple library for dealing with SAM cigar strings☆41Updated 4 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- The Genome U-Plot is a JavaScript tool to visualize chromosomal abnormalities in the Human Genome using a U-shape layout.☆32Updated 3 years ago
- ☆28Updated 8 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 8 years ago
- A web based tool to manage and automate the processing of publicly available datasets.☆39Updated 4 years ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated last month
- ☆14Updated 5 months ago
- significance testing over interval overlaps☆30Updated 5 years ago
- Enriched Domain Detector for ChIP-seq data☆16Updated 3 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago