geneinmylife / single-cell-eQTL-MR-T2D-CADView external linksLinks
☆20Sep 1, 2024Updated last year
Alternatives and similar repositories for single-cell-eQTL-MR-T2D-CAD
Users that are interested in single-cell-eQTL-MR-T2D-CAD are comparing it to the libraries listed below
Sorting:
- https://jinghuazhao.github.io/pQTLtools/☆23Mar 25, 2025Updated 10 months ago
- ☆21Aug 20, 2024Updated last year
- user-friendly pipeline for GWAS fine-mapping☆12Mar 9, 2025Updated 11 months ago
- Analysis of Global Burden of Disease data☆12Mar 15, 2021Updated 4 years ago
- INTEND (IntegratioN of Transcriptomic and EpigeNomic Data), a novel algorithm for integrating gene expression and DNA methylation dataset…☆12Dec 12, 2022Updated 3 years ago
- R package that contains plink binaries for windows, mac and linux☆14Oct 14, 2019Updated 6 years ago
- Software used to develop the TCMA database associated with 10.1016/j.chom.2020.12.001.☆14Nov 26, 2023Updated 2 years ago
- UHCA☆11Jan 23, 2025Updated last year
- Global, regional, and national prevalence and mortality burden of sickle cell disease among children and adults, 2000 - 2021: a systemati…☆14May 19, 2023Updated 2 years ago
- A software package for performing and visualising radial multivariable Mendelian randomization analyses☆12Nov 28, 2025Updated 2 months ago
- ☆13Jul 4, 2023Updated 2 years ago
- GPA: Genetic analysis incorporating Pleiotropy and Annotation☆16Feb 27, 2020Updated 5 years ago
- Code for GBMI trans-ancestry proteome Mendelian randomization satellite paper☆18Dec 25, 2023Updated 2 years ago
- A fast and programmatic MELODI☆17Apr 16, 2024Updated last year
- 🐯 tigeR: Tumor Immunotherapy Gene Expression Data Analysis R package☆54Jan 21, 2026Updated 3 weeks ago
- cfdr.pleio is an R package implementing conditional and conjunctional false discovery rates for studying pleiotropic gene variants betwee…☆18Feb 9, 2023Updated 3 years ago
- ☆20Sep 12, 2025Updated 5 months ago
- Assessing enrichment of complex disease or trait associations among QTLs☆15Jun 15, 2020Updated 5 years ago
- Code used for the GWAS-by-subtraction of non-cognitive skills and follow-up analyses☆20Jan 15, 2021Updated 5 years ago
- Fine-mapping method only using summary statistics☆20Mar 23, 2016Updated 9 years ago
- SCALLOP-INF analysis☆20Oct 24, 2025Updated 3 months ago
- This is the github repository to provide the R scripts been used in the phenome-wide Mendelian randomization study of plasma proteome.☆41Jul 3, 2021Updated 4 years ago
- Connecting GWAS summary data to analytical tools☆23Mar 25, 2024Updated last year
- ☆21Nov 15, 2024Updated last year
- Global, regional, and national burden of epilepsy, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021☆28Sep 22, 2023Updated 2 years ago
- Feature selection for preserving biological trajectories in single-cell data☆20May 29, 2025Updated 8 months ago
- A package for running MR In batches and in parallel quickly☆309Jul 25, 2025Updated 6 months ago
- ☆202Dec 24, 2023Updated 2 years ago
- Mendelian Randomization Bayesian Model Averaging☆22Feb 21, 2023Updated 2 years ago
- ☆27Aug 11, 2021Updated 4 years ago
- BulkSignalR☆26Jul 24, 2025Updated 6 months ago
- 是基础也是综合(一系列对象及函数,需要细致的讲解)☆30Apr 9, 2016Updated 9 years ago
- R package for epigraphdb☆28Jul 6, 2024Updated last year
- Transcriptomic tools to classify bladder tumours according to six published molecular classifications : Baylor, UNC, MDA, Lund, CIT-Curie…☆27Dec 21, 2022Updated 3 years ago
- Annotation of Genetic Variants☆30Dec 17, 2025Updated 2 months ago
- ☆30Oct 18, 2021Updated 4 years ago
- ☆40Jan 13, 2026Updated last month
- Linking GWAS data to analytical tools in R☆154May 20, 2022Updated 3 years ago
- shifts hg19/38 genomic position for feasible input format.☆12Jun 8, 2023Updated 2 years ago