A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing.

The article presents a survey of the rare coding variants in candidate genes in schizophrenia by deep sequencing. Topics discussed include 525 patients diagnosed of having schizophrenia, coding sequences through the use Nimblegen capture array and Illumina HiSeq paired-end sequencing at the Beijing Genome Institute (BGI) Inc., and damaging missense variants which can contribute schizophrenia etiology.