☆15Nov 17, 2025Updated 10 months ago
Alternatives and similar repositories for MENTR
Users that are interested in MENTR are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Fast manhattenplots using ggplot2☆14Apr 24, 2026Updated 4 months ago
- Python script for multivariate GWAS meta-analysis☆25Dec 6, 2024Updated last year
- GWAS-TWAS (Transcriptome-wide association study)-Pharmacological library integration pipeline☆20Mar 30, 2021Updated 5 years ago
- An R package for plotting GWAS results from the GAPIT package☆14Updated this week
- Python Scripts for Bioinformatics☆15Apr 24, 2024Updated 2 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.
- Integration of TWAS and Colocalization Analysis☆17Oct 29, 2024Updated last year
- Example for TWAS☆12Jan 23, 2022Updated 4 years ago
- Scripts for Hill et al. (2022) doi:10.1093/molbev/msac085 🟣☆11Apr 28, 2023Updated 3 years ago
- Fine-mapping with infinitesimal effects☆20May 5, 2026Updated 4 months ago
- R package for processing of GWAS output☆17Jul 9, 2024Updated 2 years ago
- ☆22Feb 19, 2025Updated last year
- ☆10Feb 25, 2024Updated 2 years ago
- TCSC (Tissue co-regulation score regression) is a statistical genetics method to identify causal tissues in diseases and complex traits.☆17Oct 3, 2024Updated last year
- Single cell Type Enrichment Analysis for Phenotypes (STEAP)☆14Jun 16, 2021Updated 5 years ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- Repository☆10Oct 23, 2024Updated last year
- ☆21Nov 15, 2024Updated last year
- This is something I have decided to do to make something good come out of the current covid situation. Here I will put the publicly avail…☆12Sep 6, 2021Updated 5 years ago
- ☆24Aug 6, 2021Updated 5 years ago
- ☆12Apr 25, 2026Updated 4 months ago
- A GWAS fine-mapping pipeline used in CAUSALdb☆27May 1, 2022Updated 4 years ago
- An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictog…☆13Jun 18, 2026Updated 3 months ago
- ☆23Sep 1, 2022Updated 4 years ago
- ☆10Apr 10, 2016Updated 10 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Toolkit for analyzing genetics data from admixed populations☆32Feb 13, 2025Updated last year
- Gene Prediction using MAKER, CEGMA, SNAP, GENEMARK & AUGUSTUS☆10Jul 20, 2017Updated 9 years ago
- Software to infer latent pleiotropic components from GWAS summary data☆17Jan 30, 2025Updated last year
- ☆10Mar 4, 2025Updated last year
- Notes by Markdown in HZAU Bioinformatics Courses☆15Dec 16, 2025Updated 9 months ago
- ☆14Aug 9, 2017Updated 9 years ago
- My R scripts, primarily R plotting scripts + some genomics software including 16S rRNA metataxnomics and RNAseq☆12Dec 19, 2022Updated 3 years ago
- GENI plots to visualise results from genome-wide association studies☆32Oct 14, 2024Updated last year
- PhenomeXcan: mapping the genome to the phenome through the transcriptome☆11Jun 28, 2020Updated 6 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- R interface to genome annotation files and the UCSC genome browser☆37Updated this week
- Data-driven signal detection for unbiased scRNA-seq data analysis☆24Jan 22, 2026Updated 7 months ago
- An accurate and efficient HLA imputation method.☆27Mar 16, 2023Updated 3 years ago
- Westlake BioBank for Chinese pilot project☆10May 17, 2023Updated 3 years ago
- ☆10May 17, 2022Updated 4 years ago
- GenomeTools: Scripts and Classes for Working with Genomic Data☆12Jun 7, 2018Updated 8 years ago
- Code used to process and analyze structural variants and short tandem repeat variants profiled in 719 deeply sequenced whole genomes as p…☆11Jun 25, 2019Updated 7 years ago