Bring Key Heme-Relevant Variants Into Focus

Current workflows for AML, MDS, and related hematological malignancy research combine multiple technologies, each contributing a different piece of the picture, and require integrating findings across separate reports. Several variant classes remain difficult to resolve, including fusion partners obscured by standard FISH and cryptic events invisible to karyotyping and targeted sequencing.

Electronic genome mapping (EGM) on the OhmX™ Platform combines structural variant detection and genome-wide copy number analysis in a single whole-genome workflow. The examples shown resolve variant classes and structural detail—including fusion partners and complex rearrangements—that fall outside the reach of karyotyping, FISH, and targeted sequencing.

Explore how EGM on the OhmX™ Platform can help you characterize the structural variants and copy number changes that current methods leave unresolved.