Scientific Presentations
dGH™ Publications & Presentations
2023: KromaTiD Webinar dGH™ The Next Generation of Metaphase FISH Techniques
2023: KromaTiD Webinar dGH in-Site™ CAR-T Kit March 13, 2023
2022: KromaTiD Presents Webinar on directional Genome Hybridization SCREEN™
2022: dGH™ Imaging and Scoring for CAS-Clover a novel high-fidelity nuclease for safe and robust generation of Tscm-enriched allogenic CAR-T cells
2022: KromaTiD Presents Webinar on directional Genome Hybridization™ with GEN News
2022: KromaTiD Presents Comprehensive Analysis of Genomic Structural Variation at Next Gen Omics in Boston
2021: Innovations in Oncology May 31st Scientist Webinar on dGH™ Analysis
2021: Life Science Tuesday – Austria
2021: Gene Therapy Online – Europe
2020: KromaTiD Presents at the 2020 Virtual NextGen Omics Series
2020: KromaTiD Presents at the 2020 Cell & Gene Therapy Virtual Congress
2019: KromaTiD Presents at the 2019 RARE Patient Advocacy Summit
Radiation and Dosimetry
Oncology
DNA Mis-Repair
Gene Editing
Genetic Diseases
Telomeres
2019: The NASA Twins Study: A Multidimensional Analysis of a Year- Long Human Space Flight
2017: Telomeres and NextGen CO-FISH: Directional Genomic Hybridization (Telo-dGH™)
2013: TERRA, hnRNP A1, and DNA-PKcs Interactions at Human Telomeres
2010: Chromosome Orientation Fluorescence in Situ Hybridization or Strand-Specific FISH.
2010: Telomere Sister Chromatid Exchange and the Process of Aging
2010: SNMIB/Apollo Protects Leading-Strand Telomeres Against NHEJ-Mediated Repair
2010: Hyper Telomere Recombination Accelerates Replicative Senescence and May Promote Premature Aging
Structural Variant Detection
2019: Directional Genomic Hybridization (dGH) for Detection of Intrachromosomal Rearrangements
2017: Telomeres and NextGen CO-FISH: Directional Genomic Hybridization (Telo-dGH™)
2013: Directional Genomic Hybridization for Chromosomal Inversion Discovery and Detection
2011: CO-FISH, COD-FISH, ReD-FISH, SKY-FISH
2010: Chromosome Orientation Fluorescence In Situ Hybridization or Strand-Specific FISH.
Clinical Relevance of Structural Variants
Supporting research from others which underscores the importance of structural variants within a clinical context
2019: Multi-Platform Discovery of Haplotype Resolved Structural Variation in Human Genomes
2019: Comprehensive Evaluation of Structural Variation Detection Algorithms for Whole Genome Sequencing
2016: Landscape of Somatic Mutations in 560 Breast Cancer Whole-Genome Sequences
2016: Frequency and Complexity of De Novo Structural Mutation in Autism
2013: Phenotypic Impact of Genomic Structural Variation: Insights from and for Human Disease
2011: Genome Structural Variation Discovery and Genotyping
2010: Structural Variation in the Human Genome and its Role in Disease