We will analyze genotyping and whole genome sequencing data
obtained
from the collected families
in
close collaboration with the sample providers.
We hope to
be able to analyze samples from across
the world and
include patients from
underrepresented populations. We will also
develop population specific reference genomes that will
improve the detection
of population
specific risk factors.
We welcome any questions about the data analysis process -
please feel free to
contact us with your queries.