A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data

Overview of attention for article published in Genome Medicine, January 2020

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In the top 25% of all research outputs scored by Altmetric
Good Attention Score compared to outputs of the same age (75th percentile)

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A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data - https://t.co/CXzTaFQsCV

@CHOP_Research A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data https://t.co/tEFOstBV9S #newresearch

RT @frapaport: A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data https://t.co/bt…

RT @4130chromo: A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data https://t.co/dW…

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