Blog Archives

An open source toolkit for repurposing Illumina sequencing systems as versatile fluidics and imaging platforms.

The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders.

Embryonic lethal genetic variants and chromosomally normal pregnancy loss.

Induction of dopaminergic neurons for neuronal subtype-specific modeling of psychiatric disease risk.

Rates of contributory de novo mutation in high and low-risk autism families.

Recent ultra-rare inherited variants implicate new autism candidate risk genes.