Hello,

we have performed a WES of a single human sample and I am interested to analyse the runs of homozygosity in this sample. Especially, I am interested to unterstand if segmental uniparental isodisomy or parental relatedness is the cause for a large homozygous region in this sample. Unfortunately, we do not have DNA of the parents.

Therefore, I need bioinformatic support and would be happy about a cooperation. Please feel free to contact me.

Thanks Andreas

More Andreas Brodehl's questions See All
Similar questions and discussions