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NGS in Precision Medicine-Oncology
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eBook
Are you interested in learning more about the impact of Next-Generation Sequencing (NGS) in Precision Medicine Oncology (PM)? Do you want to have a better understanding of how automation can help laboratories doing NGS testing within the field of Oncology?
Case Study
Are you working in precision medicine-oncology and looking to automate your NGS library preparation workflows?
In this case study, CeGaT, an innovative diagnostics company in Germany, explains the benefits of automating the workflows for NGS library preparation for the analyses of Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI).
Video
Discover how Hamilton worked with the Munich Leukemia Laboratory to develop and validate fully automated methods for NGS library preparation with the TruSeq® DNA PCR-Free and the TruSeq® Stranded Total RNA illumina’s kit
Video
See how the Hamilton Microlab® STARlet performs the Hereditary Cancer Solution (HCS) by SOPHiA GENETICS at the Clinical Genomics Laboratory of the Moderna University Hospital
Webinar
From gene to genome: Next-Generation Sequencing workflow automation. Learn about the challenges and benefits of automation through the experience of the Munich Leukemia Laboratory.
Webinar
In this Webinar, CeGaT describes the features and advantages of their automated NGS systems and illustrates the benefits of their genomic services through case studies.
