New Computational Tool for Rapid Identification of Disease-causing Variations in the Human Genome
Scientists from the University of Utah and Omicia Publish VAAST: Software to Identify Cause of Fatal Childhood Genetic Syndrome
27-Jun-2011 -
Scientists from the University of Utah and Omicia, Inc., a privately held company developing tools to interpret personal genome sequences, announced the publication in Genome Research of a new software tool called VAAST, the Variant Annotation, Analysis and Selection Tool, a probabilistic ...
genome sequences
genome sequencing
genomes
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