A needle plot for mutation data
☆27Aug 31, 2017Updated 8 years ago
Alternatives and similar repositories for muts-needle-plot
Users that are interested in muts-needle-plot are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Lollipop-style mutation diagrams for annotating genetic variations.☆199Sep 20, 2024Updated last year
- ☆13Apr 29, 2020Updated 6 years ago
- Javascript library for visualizing genomics data with D3.☆19Jan 6, 2017Updated 9 years ago
- A tool to examine duplicate read characteristics in a BAM file☆12Dec 8, 2017Updated 8 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 11 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Processing and analysis of data coming from Illumina sequencing machines☆10Apr 16, 2026Updated last week
- This project contains simple methods to measure sample relatedness and identify potential swaps and contamination☆10Jan 8, 2016Updated 10 years ago
- Parse samtools pileup file to get how many bases and what kind of bases are called☆14Apr 30, 2024Updated last year
- A python tool for parsing pedigree files☆16Aug 29, 2017Updated 8 years ago
- https://bam.iobio.io☆47Mar 29, 2026Updated last month
- INC-Seq: Accurate single molecule reads using nanopore sequencing☆16Sep 11, 2020Updated 5 years ago
- A Java package for non-invasive cancer diagnosis using methylation profiles of cell-Free DNA.☆16Apr 2, 2019Updated 7 years ago
- Web-based database system for flow cell management (incl. REST API)☆16Mar 7, 2024Updated 2 years ago
- Exon-exon splice junctions across SRA☆43Jul 30, 2021Updated 4 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- Classifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests☆50Aug 3, 2024Updated last year
- ☆26Aug 8, 2024Updated last year
- The vignette provided has a basic sketch of the steps we interactively will go through to build a package with devtools, explains version…☆11Jul 29, 2020Updated 5 years ago
- phenotype-based prioritization of candidate genes for human diseases☆64Jan 25, 2023Updated 3 years ago
- ☆12Nov 15, 2018Updated 7 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- Automatically exported from code.google.com/p/pyvttbl☆10Mar 14, 2024Updated 2 years ago
- Lollipop-diagram to interactively visualize genetic mutations☆33Sep 10, 2024Updated last year
- ☆10Jul 13, 2022Updated 3 years ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- VisCap is an open flexible, software program targeted to clinical laboratories for inference and visualization of germline copy number va…☆22Dec 13, 2019Updated 6 years ago
- ☆20Feb 24, 2017Updated 9 years ago
- Mapping of GENCODE gene annotation set files to older assembies☆13Apr 16, 2026Updated 2 weeks ago
- Barcoded Molecular Families☆22Nov 20, 2017Updated 8 years ago
- web based visualisation of molecular interaction data☆12May 22, 2025Updated 11 months ago
- Almost Idiomatic D Code☆18Nov 8, 2016Updated 9 years ago
- VCF-kit: Assorted utilities for the variant call format☆134Jul 10, 2025Updated 9 months ago
- Using reference-free compressed data structures to analyse thousands of human genomes (1000 Genomes ReadServer)☆14Sep 23, 2017Updated 8 years ago
- HGVS variant nomenclature checker☆99May 1, 2023Updated 2 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- ☆14Dec 13, 2023Updated 2 years ago
- significance testing over interval overlaps☆30Jul 11, 2020Updated 5 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Dec 23, 2023Updated 2 years ago
- Tools for next-generation sequencing analysis☆89Jun 25, 2019Updated 6 years ago
- Prioritize structural variants based on CADD scores☆29May 7, 2020Updated 5 years ago
- Horizon chart js library for DNA data.☆62Apr 30, 2016Updated 10 years ago
- SiNVICT: Ultra-Sensitive Detection of Single Nucleotide Variants and Indels in Circulating Tumour DNA☆27Oct 6, 2020Updated 5 years ago