Publication | Open Access

Clinical Validation of a Myeloid Next-Generation Sequencing Panel for Single-Nucleotide Variants, Insertions/Deletions, and Fusion Genes

Allelic VariantSequencingMedicineGeneticsNext-generation SequencingPathologySingle-nucleotide VariantsGenomicsClinical ValidationFusion GenesMolecular DiagnosticsBioinformaticsVariant Interpretation