Big Browser watching your genome
☆11Apr 10, 2016Updated 9 years ago
Alternatives and similar repositories for BigBrowser
Users that are interested in BigBrowser are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- simple viewer for variant call format using htslib☆33Jan 17, 2017Updated 9 years ago
- CutePeaks is a standalone Sanger trace viewer steered by a modern and user-friendly UI.☆46Jun 26, 2025Updated 8 months ago
- Materials for http://dib-training.readthedocs.org/en/pub/2015-11-09-docker.html☆14May 29, 2017Updated 8 years ago
- ☆63Sep 21, 2016Updated 9 years ago
- R Bindings for htslib/bcf☆10Oct 4, 2023Updated 2 years ago
- FastQC port to Qt5: A quality control tool for high throughput sequence data.☆113Aug 4, 2020Updated 5 years ago
- Arkanosis' configuration files☆20Feb 26, 2026Updated 3 weeks ago
- A simple and performant API for working with many genomic file formats in a consistent fashion☆16Mar 23, 2018Updated 8 years ago
- Genevieve client: using GenNotes, report ClinVar for individual genomes & add consensus notes☆10Aug 2, 2016Updated 9 years ago
- The open source version of the Melbourne Genomics Health Alliance Exome Sequencing Pipeline☆33Jan 20, 2018Updated 8 years ago
- next gen ADAP☆12Jan 28, 2020Updated 6 years ago
- WebApp for DNA variants interpretation☆15Mar 18, 2026Updated last week
- Plot allele frequencies in VCF files☆11Jun 4, 2019Updated 6 years ago
- Boiler: a software tool for highly efficient, lossy compression of RNA-seq alignments☆13Jul 14, 2016Updated 9 years ago
- HTML5 canvas genomic graphics library☆76May 6, 2019Updated 6 years ago
- Clin.iobio - Workflow and reporting for iobio variant analysis pipeline☆12Oct 7, 2025Updated 5 months ago
- Code snippets that I used in blog posts at https://www.katzentante.at☆14Sep 9, 2022Updated 3 years ago
- Visualizing genetic sequence variation☆13Apr 27, 2020Updated 5 years ago
- Write-once-read-many table for large datasets.☆27Oct 5, 2023Updated 2 years ago
- The Exome Coverage and Identification Report displays the coverage of every target region in your capture design. It also displays regio…☆14Apr 22, 2015Updated 10 years ago
- CNV calling algorithm for detection of homozygous and hemizygous deletions from whole exome sequencing data☆12Nov 9, 2025Updated 4 months ago
- Ribosome profiling analysis framework as described in de Klerk E., Fokkema I.F.A.C et al (2015). Alignment, triplet periodicity analysis,…☆12May 16, 2023Updated 2 years ago
- iOS port for serval chat app☆11Nov 15, 2018Updated 7 years ago
- Python Localstack Examples☆11Mar 3, 2026Updated 3 weeks ago
- Splicing Prediction Pipeline☆14Aug 12, 2023Updated 2 years ago
- Pipeline to filter whole exome vcf files and generate a report document for clinical diagnostics.☆14Nov 11, 2019Updated 6 years ago
- Web-based database system for flow cell management (incl. REST API)☆16Mar 7, 2024Updated 2 years ago
- a bucket of bioinformatics scripts☆13Mar 5, 2026Updated 2 weeks ago
- A simple observation count database☆11Jan 13, 2026Updated 2 months ago
- Distributed machine learning platform☆13Aug 20, 2015Updated 10 years ago
- MEDOC is a free python wrapper to clone MEDLINE into local mySQL database☆23Mar 18, 2026Updated last week
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆22Sep 7, 2019Updated 6 years ago
- Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores …☆16Aug 9, 2018Updated 7 years ago
- A simple linux sheel cheat sheet☆20Mar 15, 2019Updated 7 years ago
- BioDSL (pronounced Biodiesel) is a Domain Specific Language for creating bioinformatic analysis workflows.☆16Jul 30, 2018Updated 7 years ago
- A library to assist with a variety of -omic analyses. Included are tools for proteomics, transcriptomics, and genomics.☆16Aug 3, 2023Updated 2 years ago
- Mapped QC analysis program☆44May 16, 2018Updated 7 years ago
- ☆17Aug 31, 2017Updated 8 years ago
- The Loss-of-Function ToolKit (LoFTK) allows efficient and automated prediction of LoF variants from both genotyped and sequenced genomes,…☆10Jul 30, 2025Updated 7 months ago