LongVar low-coverage data

This dataset includes sequencing data from participants of the LongVar study. Specifically, it comprises low-coverage whole genome sequencing (WGS) data which was derived from cell-free DNA from blood samples. These data were generated to compare imputation accuracy. 133 individuals agreed to share their data, and are healthy volunteers.

Type: Whole Genome Sequencing
Archiver: European Genome-Phenome Archive (EGA)

1 Dataset 1 Publication

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID	Description	Technology	Samples
EGAD50000001607	This dataset includes sequencing data from participants of the LongVar study. Specifically, it comprises low-coverage whole genome sequencing (WGS) data which was derived from cell-free DNA from blood samples. These data were generated to compare imputation accuracy. 133 individuals agreed to share their data, and are healthy volunteers.	Illumina NovaSeq 6000	133

Publications	Citations
Genotype imputation from low-coverage data for medical and population genetic analyses. Biagini SA, Becelaere S, Aerden M, Jatsenko T, Hannes L, Van Damme P, Breckpot J, Devriendt K, Thienpont B, Vermeesch JR, Cleynen I, Kivisild T. Genome Res 35: 2025 1929-1941	0