We spoke with him about his program for rapidly sequencing
the genomes of sick children and what he's looking for in the field of next generation sequencing and genomics.
Not exact matches
As techniques to analyze whole
genomes improve, more autism - associated mutations will be discovered, clarifying the genetic basis
of the disease, says Stephen Scherer, a geneticist at The Hospital for
Sick Children in Toronto who helped run the international study.
In work published in August in the Proceedings
of the National Academy
of Sciences and presented today, researchers from the Hospital for
Sick Children in Toronto, Canada, studied 11 families with Li - Fraumeni syndrome and reported that those affected had an average
of 12 CNVs in their
genome, compared with three in controls.