Public release of the work on the associations of Structural Variants with AD and ADRD traits

A program for the analysis of single cell nanopore long read data

Toolkit for genome-wide analysis of tandem repeats

Tools for merging Tandem Repeat VCF files

MA-FOCUS: Multi-Ancestry Fine-mapping Of CaUsal gene Sets

diploid SNV caller for error-prone reads

Low Coverage Calling of Genotypes

Raw nanopore signal mapper that enables real-time targeted sequencing

CLI tool for flexible and fast adaptive sampling on ONT sequencers

Pangolin is a deep-learning method for predicting splice site strengths.

Just the leafviz parts of Leafcutter

Nanopore RNA-Seq data from the Singapore Nanopore-Expression Project

BigWig and BAM utilities

Tissue-specific variant effect predictions on splicing

Multi-Omic Strategies for TWAS

Cell type specific enhancer-gene predictions using ABC model (Fulco, Nasser et al, Nature Genetics 2019)

Repository for commands used for the Swan manuscript

A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data

dbSNP

Annotation and Ranking of Structural Variation

Make Complex Heatmaps