astheeggeggs / BipExView external linksLinks
☆10Jul 2, 2024Updated last year
Alternatives and similar repositories for BipEx
Users that are interested in BipEx are comparing it to the libraries listed below
Sorting:
- Detect key Units in mosaic Tandem Repeats from representative reads from the same locus☆11Aug 2, 2023Updated 2 years ago
- A single-cell RNAseq differential expression analysis approach in case-control study☆10Mar 6, 2022Updated 3 years ago
- Pleiotropy-informed conditional and conjunctional false discovery rate☆36Jun 3, 2025Updated 8 months ago
- As part of the COVID-19 Host Genetics Global initative, this repo serves to corroborate sample scripts for sequencing QC.☆12Jul 30, 2020Updated 5 years ago
- R package enabling statistical association analysis and using immunogenetic data transformation functions for HLA amino acid fine mapping…☆14Jan 31, 2024Updated 2 years ago
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- genetic correlation between phenotypes in the UK biobank☆13Feb 22, 2024Updated last year
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 6 years ago
- Repository for RecallME-v.0.1 a variant calling pipelines benchmarker and optimizer☆13Dec 18, 2023Updated 2 years ago
- ☆15Aug 22, 2023Updated 2 years ago
- Exome Copy Number Variation Polisher via Deep Learning☆18Jun 1, 2020Updated 5 years ago
- ☆16Jan 10, 2022Updated 4 years ago
- Scripts to reproduce TrioBinning manuscript☆17Mar 31, 2020Updated 5 years ago
- An R package for generating comparative regional association plots☆18Sep 30, 2025Updated 4 months ago
- A package for MR Practical Sessions☆20Apr 15, 2020Updated 5 years ago
- R package for investigating clustered heterogeneity in Mendelian randomization (MR) analyses.☆17Oct 15, 2021Updated 4 years ago
- Combine structural variation outputs from long sequencing reads into a superior call set☆18Aug 6, 2025Updated 6 months ago
- Analysis and figure generation code for the ABRF NGS Phase II Study on DNA-seq reproducibility☆18Aug 5, 2021Updated 4 years ago
- Characterization of Structural Variation in Chinese samples☆18Dec 22, 2021Updated 4 years ago
- Methods and analysis for Garcia-Nieto, et al. Somatic mutations☆16Jan 5, 2020Updated 6 years ago
- Code used for the GWAS-by-subtraction of non-cognitive skills and follow-up analyses☆20Jan 15, 2021Updated 5 years ago
- Phase reads, assemble haplotypes and detect SVs☆19Nov 11, 2020Updated 5 years ago
- Code accompanying Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes☆44Apr 16, 2021Updated 4 years ago
- HLA-TAPAS pipeline for HLA association and fine-mapping studies☆54Dec 19, 2023Updated 2 years ago
- ☆11Jul 3, 2022Updated 3 years ago
- Code accompanying The Evolutionary history of 2,658 cancers☆47Apr 16, 2021Updated 4 years ago
- Ultra-fast, high-performing structural variation (SV) detector☆24Apr 26, 2023Updated 2 years ago
- ☆23Apr 14, 2022Updated 3 years ago
- ☆22Sep 17, 2025Updated 4 months ago
- A Deep Learning Model for Predicting Next-Generation Sequencing Depth from DNA Sequence☆23Jul 8, 2021Updated 4 years ago
- Toolkit for VNTR genotyping and repeat-pan genome graph construction☆31Aug 18, 2025Updated 5 months ago
- ☆24Nov 27, 2024Updated last year
- Regional association plots☆24Apr 1, 2024Updated last year
- CARE: Context-Aware Read Error correction for Illumina reads☆21Nov 1, 2023Updated 2 years ago
- A method for measuring chromosome-specific telomere length from long reads☆22May 20, 2024Updated last year
- The cattle Genotype-Tissue Expression atlas v1☆28Mar 14, 2023Updated 2 years ago
- Versatile simulator for structural variance and Nanopore/PacBio sequencing reads☆28Aug 21, 2025Updated 5 months ago
- Specification for the GWAS-VCF format (manuscript in preparation)☆26Aug 3, 2021Updated 4 years ago
- Method to optimally select samples for validation and resequencing☆30Apr 6, 2021Updated 4 years ago