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Rare Genomics Institute's Science Challenge Winners to Use Omicia’s Clinical NGS Interpretation Software
The annual BeHEARD Rare Disease Science Challenge provides donated biotechnology prizes to research investigators. This year’s Challenge winners include three investigators who will use the Opal genome informatics and variant interpretation software to further their studies of underrepresented diseases.
#PrecisionMedicine #Genomics #ClinicalNGS  

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Automated, Algorithmic Approaches to Variant Interpretation
Traditional methods for the clinical interpretation of genetic variants to find the cause of a disease are often ineffective and inefficient.. Omicia describes an automated approach that significantly increases the likelihood of diagnosing genetic disease.

#PrecisionMedicine #Genomics #ClinicalSequencing

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Omicia, the leading clinical genomics and informatics company, today announced that it has been selected by Genomics England to provide clinical interpretation services for the 100,000 Genomes Project.
#PrecisionMedicine  #Genomics   #ClinicalSequencing
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