Family-Based Whole-Genome Sequencing Reveals Candidates for Mendelian Disease
Roach, Glusman et al., Science
Researchers at the Institute for Systems Biology and Complete Genomics have identified candidate disease-causing genes for Miller syndrome and ciliary dyskinesia, both Mendelian disorders. They sequenced the genomes of a family of four, allowing them to determine recombination sites with precision (at 99.999 percent accuracy) and identify rare single-nucleotide polymorphisms. "Our results demonstrate the unique value of complete genome sequencing in families," the authors write.
Accelrys Taps Content Management Software Exec as New CEO, Reaffirms Commitment to Life Sciences
The company will continue to develop additional capabilities for its scientific informatics platform, "including advanced portal deployment to make our predictive science, scientific business intelligence, and data management tools more accessible for scientists and engineers."
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