LiuzLab / AI_MARRVEL
AI-MARRVEL (AIM) is an AI system for rare genetic disorder diagnosis
☆12Updated 3 weeks ago
Alternatives and similar repositories for AI_MARRVEL:
Users that are interested in AI_MARRVEL are comparing it to the libraries listed below
- Genomic Identification of Significant Targets in Cancer (GISTIC), version 2☆51Updated 3 years ago
- MutSig2CV from Lawrence et al. 2014☆31Updated 4 years ago
- Rareservoir Database Tools☆15Updated 2 years ago
- Fork from https://bitbucket.org/mcgranahanlab/lohhla/src, modified for MSKCC needs☆30Updated last year
- A comprehensive, accurate and efficient solution for analysis of large scale base-resolution DNA methylation data☆16Updated 3 years ago
- ☆16Updated 3 years ago
- Benchmarking of CNV calling tools☆18Updated 5 years ago
- Assign gene names to regions in a BED file☆24Updated last year
- A modular, containerized pipeline for ATAC-seq data processing☆57Updated last month
- ☆28Updated last year
- Comprehensive genome-wide visualization of absolute copy number and copy neutral variations☆29Updated 6 years ago
- cfSNV: An R tool of sensitively detecting tumor mutations from cell-free DNA in blood☆11Updated last year
- ☆21Updated last week
- This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination …☆34Updated 9 months ago
- ☆25Updated 5 years ago
- tools to find circRNAs in RNA-seq data☆42Updated 7 years ago
- Public repository containing research code for the TCGA PanCanAtlas Splicing project☆41Updated 4 years ago
- Main repository for Drews et al. (Nature, 2022)☆39Updated last year
- Fork of the Polysolver project☆31Updated 5 years ago
- ⛏ HLA predictions from NGS shotgun data☆53Updated last week
- A computational workflow for exitron splicing identification☆12Updated 7 months ago
- A fast and robust pre-processing pipeline for bulk or single-cell whole-genome bisulfite sequencing (WGBS) data.☆35Updated 3 years ago
- Comprehensive analysis of small RNA sequencing data☆31Updated 10 months ago
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆25Updated 7 months ago
- ☆23Updated last year
- All-FIT - Allele-Frequency-based Imputation of Tumor Purity☆17Updated 5 years ago
- Ethnicity Annotation from Whole-Exome and Targeted Sequencing Data☆16Updated 2 years ago
- Quantitation and visualization of differential alternative splicing events☆10Updated last year
- RNA editing quantification in deep transcriptome data☆15Updated 2 years ago
- An R package for predicting HR deficiency from mutation contexts☆28Updated 2 months ago