Pipeline to perform annotation of variants to a pre-selected set of pathways and then calculate and associate pathway-specific Polygenic Risk Scores (PRS) and typical PRS.

Automated Validation of CNV calls from SNPs array

In order to address the concerns regarding the privacy of genetic data and the need to perform genotype imputation relying on a server that is located in the United States, we have developed a pipe…

SNPbrowser is project written in python to display results from Genome-Wide Association Studies (GWAS) with a wide range of possibilities, including overlap of multiple studies.

R script to calculate Polygenic Risk Score from genotype data, and eventually plot them.

Tandem REpeat Annotation Toolkit (TREAT)

Generic targeted local assembler and genotyper for long-read data

a python package for finding tandem repeats from genomic sequences

A tool for motif annotation and visualization in tandem repeats.