Alignments and imputed variants for the following manuscript: "Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates", bioRxiv DOI: https://doi.org/10.1101/2022.12.07.519512

This repository contains the alignments to GRCh37 and genome-wide imputed variants for the low pass sequence data generated as part of the following manuscript: https://doi.org/10.1101/2022.12.07.519512. See manuscript for further details.