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Gene Fusion Workshops

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Showing 13–24 of 50 categories
Data Interpretation and Reporting
Professional development course for laboratory directors and genetic counselors on interpreting fusion detection results and communicating findings to clinicians.
3+WORKSHOPS
PROGRAMMES
Interpreting Gene Fusion Data from RNA Sequencing Clinical Reporting Standards for Detected Gene Fusions Visualizing Complex Gene Fusion Breakpoints Effectively +2 more programmes
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Fusion Gene Nomenclature and Standards
Compliance training ensuring laboratory professionals understand HGNC nomenclature standards and proper reporting conventions for gene fusion findings.
3+WORKSHOPS
PROGRAMMES
HUGO Nomenclature Rules for Fusion Genes Standardizing Fusion Gene Nomenclature in Reports Breakpoint Nomenclature and Transcript Variant Notation +2 more programmes
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CLIA Compliance for Molecular Testing
Regulatory training for laboratory managers on maintaining CLIA certification standards when offering gene fusion detection as a clinical diagnostic service.
3+WORKSHOPS
PROGRAMMES
CLIA Compliance Documentation Audit Framework Analytical Validation Protocols for Fusion Detection Quality Management System Implementation for Molecular Labs +2 more programmes
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Whole Genome Sequencing Analysis
Advanced bioinformatics training teaching analysts how to extract fusion gene information from whole genome sequencing datasets and integrate with clinical data.
3+WORKSHOPS
PROGRAMMES
Identifying Gene Fusion Events in WGS Data RNA-Seq Validation of Putative Fusion Transcripts Structural Variant Calling and Fusion Gene Annotation +2 more programmes
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Multiplexed Fusion Detection Assays
Technical workshop for laboratory technicians on developing and implementing multiplex PCR and qPCR assays detecting multiple fusion genes simultaneously.
3+WORKSHOPS
PROGRAMMES
Designing Multiplexed PCR Assays for Fusion Detection Digital Droplet PCR for High Sensitivity Fusion Quantification Next Generation Sequencing Panel Design and Analysis Workflows +2 more programmes
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Sanger Sequencing Confirmation Methods
Hands-on training teaching technicians how to use Sanger sequencing as a gold-standard confirmation method for suspected gene fusion events.
3+WORKSHOPS
PROGRAMMES
Sanger Sequencing for Gene Fusion Detection Breakpoint Validation Through Sanger Protocol High Throughput Sanger Confirmation for Fusions +2 more programmes
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Fusion Gene Database Management
Information technology training for laboratory staff on managing, curating, and updating fusion gene knowledge databases for clinical decision support.
3+WORKSHOPS
PROGRAMMES
Fusion Gene Data Integration and Curation Breakpoint Annotation and Structural Variant Mapping Query Optimization for Fusion Gene Archives +2 more programmes
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Long-Read Sequencing Technologies
Advanced training for genomic scientists on utilizing long-read sequencing platforms like PacBio and Nanopore for full-length fusion transcript characterization.
3+WORKSHOPS
PROGRAMMES
Detecting Gene Fusions Using Long-Read Sequencing Oxford Nanopore Sequencing for Fusion Transcript Analysis PacBio HiFi Reads for Cancer Gene Fusion Discovery +2 more programmes
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Bioinformatics Tool Software Training
Practical software training for analysts on commercial and open-source bioinformatics tools specifically designed for fusion gene discovery and analysis.
3+WORKSHOPS
PROGRAMMES
Identifying Gene Fusion Events with FusionCatcher STAR-Fusion Pipeline for Oncology Applications Arriba Gene Fusion Detection and Annotation +2 more programmes
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Gene Fusion Prognosis and Clinical Significance
Clinical education program teaching pathologists and clinicians how to assess the prognostic and therapeutic significance of detected gene fusions.
3+WORKSHOPS
PROGRAMMES
Identifying Pathogenic Gene Fusions in Cancer Gene Fusion Breakpoint Analysis and Interpretation Prognostic Stratification Using Gene Fusion Data +2 more programmes
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RNA Extraction Optimization Techniques
Laboratory skills training for technicians on optimizing RNA extraction protocols to preserve fusion transcript integrity for downstream analysis.
3+WORKSHOPS
PROGRAMMES
Advanced RNA Extraction Protocol Optimization Magnetic Bead Based RNA Isolation Methods RNA Quality Assessment and Troubleshooting +2 more programmes
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Copy Number Variation Analysis
Intermediate bioinformatics training teaching analysts how to detect and analyze copy number variations associated with gene fusion events.
3+WORKSHOPS
PROGRAMMES
CNV Detection and Breakpoint Mapping Techniques Quantitative PCR for Fusion Gene Validation FISH and Cytogenetic Approaches for CNV Characterization +2 more programmes
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