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.
Rosetta Genomics' Q2 Net Loss Rises 62 Percent
Rosetta's loss rose sharply on increased SG&A spending and losses associated Parkway Clinical Labs, which the firm recently sold. It also announced plans for a cleantech division.
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