An R HTMLWidget for making interactive manhattan plots for GWAS.
☆20Aug 1, 2015Updated 10 years ago
Alternatives and similar repositories for D3ManhattanPlots
Users that are interested in D3ManhattanPlots are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Visualization methods for omics dataset quality control☆10Jul 17, 2025Updated 8 months ago
- ☆13May 16, 2016Updated 9 years ago
- Canonical SGE cluster genotype imputation pipeline☆12Jan 18, 2016Updated 10 years ago
- Transfer coordinates across genomes☆23Mar 19, 2026Updated last week
- A list of cool software for genetic analysis and the like☆12Sep 21, 2018Updated 7 years ago
- NordVPN Threat Protection Pro™ • AdTake your cybersecurity to the next level. Block phishing, malware, trackers, and ads. Lightweight app that works with all browsers.
- OpenMendel package for haplotyping and imputation☆25Oct 8, 2025Updated 5 months ago
- FM-index for full-text search☆20Nov 20, 2021Updated 4 years ago
- AlignerBoost is a generalized software toolkit for boosting Next-Gen sequencing mapping precision using a Bayesian based mapping quality …☆11Mar 1, 2022Updated 4 years ago
- ...for people who don't like wasting time typing git commands☆21Mar 2, 2021Updated 5 years ago
- ☆12May 8, 2021Updated 4 years ago
- ☆18Dec 1, 2017Updated 8 years ago
- MeGAMerge (A tool to merge assembled contigs, long reads from metagenomic sequencing runs)☆14Dec 7, 2016Updated 9 years ago
- An application to compare genetic maps with D3 & Shiny☆22Feb 28, 2023Updated 3 years ago
- ☆19Nov 21, 2024Updated last year
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- Lightweight-Productive-Reliable parallel task running and results aggregation (MapReduce on multicore)☆10Jun 10, 2018Updated 7 years ago
- [deprecated] P-value adjustment methods for multiple testing correction☆16Nov 25, 2016Updated 9 years ago
- A coalescent simulator for genome-scale sequences☆44Jan 2, 2024Updated 2 years ago
- Trying to make the largest repository of deeplearnjs example code☆10Aug 19, 2019Updated 6 years ago
- exprAnalysis☆15Dec 19, 2016Updated 9 years ago
- small scripts, functions or bits of code for parsing genomic data☆14Sep 24, 2022Updated 3 years ago
- Versatile tool for detecting selective sweeps with a variety of ages, strengths, starting allele frequencies, and completeness.☆15Feb 16, 2026Updated last month
- ☆24Jul 29, 2025Updated 7 months ago
- RRSelection: A linkage disequilibrium method to detect selection region across population VCF☆14Feb 11, 2019Updated 7 years ago
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- Rust implementation of Flavia95's GFAtoVCF☆16Jan 17, 2022Updated 4 years ago
- A comprehensive pipeline for post-GWAS analysis leveraging diverse types of omics data☆29Aug 2, 2022Updated 3 years ago
- FASTAptamer: A Bioinformatic Toolkit for High-Throughput Sequence Analysis of Combinatorial Selections☆10Oct 7, 2024Updated last year
- TEMP is a software package for detecting transposable elements (TEs) insertions and excisions from pooled high-throughput sequencing dat…☆22Jul 31, 2017Updated 8 years ago
- TEFLoN uses paired-end illumina sequence data to discover and genotype transposable elements present in your samples.☆13Mar 5, 2021Updated 5 years ago
- TQSLE v1.0 released☆10Aug 29, 2023Updated 2 years ago
- ClaMSA (Classify Multiple Sequence Alignments).☆13Nov 21, 2024Updated last year
- A toolkit to calculate polygenic scores using PLINK2, PRS-CS, RapidoPGS, or PRSice2.☆16Aug 16, 2024Updated last year
- A collection of well-known bioinformatics programs.☆25Apr 24, 2015Updated 10 years ago
- 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.
- Convert structural variants to sequence graphs [ VCF + FASTA ---> GFA ]☆11Mar 6, 2024Updated 2 years ago
- Package Objects☆12Jun 5, 2025Updated 9 months ago
- Align subreads to ccs reads☆14Jun 11, 2025Updated 9 months ago
- ARCHIVED☆30May 10, 2022Updated 3 years ago
- A tool for sniffing out the differences in vari-Ants☆38Jan 28, 2026Updated last month
- This is a basic repository with all the scripts necessary to reconstruct the data analysis from our work on the 200 Genomes☆12Aug 31, 2018Updated 7 years ago
- UCSC liftOver (genome build converter) for vcf format☆12Nov 29, 2017Updated 8 years ago