AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting

Overview of attention for article published in BMC Medical Genomics, February 2020

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AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting https://t.co/6LY4FFmunY https://t.co/QkloeNi7C7

16 Feb 2022

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AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting. https://t.co/LkEC3MmMtE #diagnosticreport #genomics #mutationdatabase #NGSsequencing #variantannotation @ncbi https://t.co/OZwCVwSx2

08 Feb 2020

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New article: AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting. https://t.co/9HDRFM8sI2 #MDS #mdssm #hematology

06 Feb 2020

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RT @jsantoyo: AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting. h…

05 Feb 2020

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