Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data

Overview of attention for article published in BMC Genomics, May 2021

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RT @jsantoyo: Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data. #NGS #…

RT @jsantoyo: Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data. #NGS #…

RT @jsantoyo: Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data. #NGS #…

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