By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – The Wellcome Trust announced today that is undertaking a three-year project to sequence whole genomes or exomes from 10,000 individuals in the UK with an eye towards finding genetic variants — including rare variants — involved in disease.

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In this webinar, the first in the “New Frontiers in Liquid Biopsy Research” series, Bea Bellosillo, head of pathology at the Hospital del Mar, will discuss her experience evaluating an early-access lung cancer panel that detects copy number variants and fusions.