Institute for Systems Biology Uses Complete Genomics, Inc. Human Genome Sequencing Service to Verify Gene Responsible For Miller Syndrome; Results Published in Science

Published: Mar 11, 2010

MOUNTAIN VIEW, Calif.--(BUSINESS WIRE)--Complete Genomics Inc., a third-generation human genome sequencing company, today announced that the Institute for Systems Biology (ISB) employed Complete Genomics’ human genome sequencing service to sequence a family quartet to determine the depth of genetic information possible in analyzing a full family’s sequence, and to verify the gene responsible for Miller syndrome, a rare craniofacial disorder. Results from this collaboration will be published online later today in the journal Science; the manuscript is titled “Analysis of Genetic Inheritance in a Family Quartet by Whole Genome Sequencing.”

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