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May 10, 2012 Omicia Provides Early Access to Powerful Solution for Individual Genome Interpretation [Business Wire]
April 25, 2012 Omicia and University of Utah wins prestigious Bio-IT Best Practices Award [Bio-IT World]
November 1, 2011 Next-Gen Tools Have Near-Term Applications in the Clinic, Companies Say [GenomeWeb]
November 2011 Personal Account of the Discovery of a New Disease Using Next-Generation Sequencing [Future Medicine]
October 11, 2011 Businesses Ready Whole-Genome Analysis Services for Researchers [Nature Medicine]
July 1, 2011 Omicia, U of Utah Researchers Use Integrated Approach to Improve Disease-Gene Searching [BioInform]
June 30, 2011 A Tragic Case And A Genomic Hope [Forbes]
June 29, 2011 Following Proof of Concept for Algorithm, Omicia Preps Launch of Clinical Genome Analysis Platform [GenomeWeb]
June 28, 2011 A New Tool for Personal Genomics [Genetic Engineering News]
June 24, 2011 Utah Researchers Find Mutation That Kills Baby Boys [Salt Lake Tribune]
June 24, 2011 Software Used to Identify Rare Genetic Disorder; Could Impact Diagnosis [Smart Planet]
June 23, 2011 VAAST Potential for New Genome Mutation Hunting Software [Bio-IT World]
June 23, 2011 Software pinpoints cause of mystery genetic disorder [Nature]
June 23, 2011 Next-Generation Gene Sequencing Brings Personal Genomics Closer, IDs Mutation in New Syndrome [Press Release]
June 23, 2011 Computational Software Provides Rapid Identification of Disease-Causing Gene Variations [Press Release]
May 13, 2011 DNA Sequencing: Beating Moore’s Law Since January 2008 [Forbes]
April 1, 2011 New Study Reveals 1 Million Human Genome Sequence Errors Across Two NGS Platforms [Bio-IT World]
September 28th, 2010 The $1,000,000 Genome Interpretation [Bio-IT World]
July 13th, 2010 Omicia Readies Technology to Interpret Human Genomes for Clinical Projects [In Sequence]
June 25th, 2010 Omicia to Put Annotation Tools To Work Analyzing Sequence Data for Genomic Cancer Care Alliance [Bioinform]
June 3rd, 2010 Omicia Joins New Genomic Cancer Care Alliance Formed to Study Whole-Genome Sequencing in Cancer Treatment [Press Release]

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