NEW YORK (GenomeWeb) – Canadian company Fusion Genomics aims to change the way infectious disease is diagnosed using a platform that it claims can capture and identify the genomes of more than 1,400 known human pathogens.
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Sequencing workflows require library quantification and normalization to ensure data quality and reduce cost.
This webinar will present the utility of a personalized in silico analytical approach for the routine clinical diagnosis of channelopathies and cardiomyopathies.
This webinar will discuss novel long-read transcript sequencing (LRTseq) methods for transcriptome annotation that could increase the efficiency and accuracy of future sequencing projects.