An R package for hierarchical clustering with p-values
☆49Dec 5, 2019Updated 6 years ago
Alternatives and similar repositories for pvclust
Users that are interested in pvclust are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Rapid Annotation Transfer Tool☆10May 21, 2025Updated 11 months ago
- LLM-based gene function enrichment tool☆18Feb 19, 2025Updated last year
- The integrated pipeline for Indel detection☆17Apr 29, 2018Updated 8 years ago
- Ruby library for handling GFA files☆17Jul 10, 2025Updated 9 months ago
- accessory functions for processing microbial community data☆12Dec 24, 2022Updated 3 years ago
- Serverless GPU API endpoints on Runpod - Get Bonus Credits • AdSkip the infrastructure headaches. Auto-scaling, pay-as-you-go, no-ops approach lets you focus on innovating your application.
- GAPPadder is tool for closing gaps on draft genomes with short sequencing data☆28Jun 1, 2017Updated 8 years ago
- Generate mutated sequence files from a reference genome.☆11Dec 26, 2022Updated 3 years ago
- Reading ASD Binary Files in R☆14Sep 13, 2017Updated 8 years ago
- ☆15May 27, 2025Updated 11 months ago
- IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split …☆16Aug 22, 2023Updated 2 years ago
- ☆14Sep 11, 2023Updated 2 years ago
- MetaProFi is a bloom filter based tool for storing and querying sequence data for accurate identification of functionally relevant geneti…☆13Apr 14, 2022Updated 4 years ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Sep 12, 2018Updated 7 years ago
- Book on Dynamical Systems Approaches to Infectious Disease Epidemiology☆11Nov 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.
- Toolkit for single-cell analysis of chromatin accessibility☆12Feb 27, 2020Updated 6 years ago
- Python module and utility programs for working with GFF files☆33Nov 25, 2020Updated 5 years ago
- HaploSweep is a method for detecting and categorizing soft and hard selective sweeps based on haplotype structure.☆11Sep 24, 2024Updated last year
- A Scalable GPU-Based Whole Genome Aligner, published in SC20: https://doi.ieeecomputersociety.org/10.1109/SC41405.2020.00043☆72Aug 7, 2024Updated last year
- Série de hackathons pour la reproductibilité - Une action MaDICS ReproVirtuFlow☆12Apr 20, 2020Updated 6 years ago
- ☆10Aug 21, 2025Updated 8 months ago
- Command line tools for IntSpan related bioinformatics operations☆12Apr 9, 2025Updated last year
- ☆17May 5, 2020Updated 6 years ago
- One-liner for mapping orthologous genes in both R and python using ENSEMBL BioMART