Genomics References

 

Therapeutic/
Disease 

Title

Journal

Conference

CAR T

Multiplexed Quantification of CAR-T Subtypes by PCR

 

AAPS:NBC

MDS

Assessing Clonal Evolution of Myeloid Neoplasms by Flow Cytometry Guided, Cell-Enriched Next Generation Sequencing

 

AACR

CAR T

A Universal Approach for Generation of Robust CAR-agnostic Calibrators for qPCR Quantification

 

WIRB 

N/A

Modular ddPCR assay design for highly sensitive single nucleotide variant detection

 

AACR

heme

Monitoring of Tisagenlecleucel Transgene DNA Using a Quantitative Polymerase Chain Reaction Assay

Molecular Therapy Methods & Clinical Development

 

Pan tumor

Optimizing reference mixture samples for bioinformatics pipeline assessment on variant calling detection for cancer diagnostics and treatment

 

AMP

AML (heme)

Evaluating machine learning methods for accurate variant calling detection on acute myeloid mutation analysis

 

AMP

Pan tumor

Noise reduction using a positional variant-dependent error model for the detection of low frequency variants in a pan-cancer next-generation sequencing panel

 

AMP

Solid tumor

Detection of Low-Frequency Variants in Minimal Residual Disease (MRD) Monitoring of Acute Myeloid Leukemias

 

AMP

Melanoma

Effects of melanin on NanoString gene and miRNA expression assays for utilization in biomarker analysis for melanoma

 

AACR

Pan tumor

Multi-omic single cell sequencing for deep cell immune profiling and identification of potential biomarkers for cell therapy and immunotherapy

 

AACR

Solid Tumor

Accelerating Oncology Drug Development by Patient Stratification

 

World Pharma Week 

Melanoma

Adjuvant dabrafenib plus trametinib versus placebo in patients with resected, BRAFV600-mutant, stage III melanoma (COMBI-AD): exploratory biomarker analyses from a randomised, phase 3 trial

Lancet Oncology

 

Pan Tumor

SABPA Chair - SABPA Frontiers in Therapeutics and Diagnostics (FTD)

 

SABPA Frontiers in Therapeutics and Diagnostics (FTD) Forum 

Breast

Development and Characterization of PTEN IHC Assay for Testing Breast Cancer Patients Specimens 

 

SABCS

AML

FLT3 inhibitors added to induction therapy induce deeper remissions 

Blood

 

AML

Identification of Low-Frequency Variants in AML Populations 

 

AMP

Solid Tumor

Evaluation of Illumina TSO500 Performance in Clinically Significant Sample Types and Input Levels 

 

AMP

Breast

Biomarker Selection of Cancer Patients for treatment with FGFR TKI

 

AMP

Heme

Enabling oncology drug approval by successful development of companion diagnostics

 

Biomarkers and Precision Medicine Conference

AML

FLT3-Explorer: A Bioinformatics Pipeline for Detecting Low Signal in FLT3 Internal Tandem Duplications in Acute Myeloid Leukemia

 

AACR

Breast

“Fit-for-Purpose” PIK3CA Assays for Patient Stratification in Breast Cancer Clinical Trials

 

AACR

Heme/Solid

Characterization of T Cell Clonality and Tumor Mutation Burden Utilizing the TCRSeq NGS and the Comprehensive NGS Assays

 

AACR

Heme 

Comparison of commercially available myeloid next-generation sequencing assays

 

AACR

AML

Development of a Novel Next-Generation Sequencing (NGS)-Based Assay for Measurable Residual Disease (MRD) in FLT3-ITD Acute Myeloid Leukemia (AML) and Its Potential Clinical Application in Patients

 

AACR

Solid

Progress toward non-invasive oncology diagnostics: Evaluation of cfDNA next-generation sequencing assays

 

AACR

AML

Development of a Novel Next-Generation Sequencing (NGS)-Based Assay for Measurable Residual Disease (MRD) in FLT3-ITD AML and Its Potential Clinical Application in Patients Treated With Chemotherapy Plus FLT3 Inhibitors. 

 

ASH

Multiple

Assessment of Pre-Analytical Effects on RNA Sequencing

 

AMP

NSCLC

Optimization of testing methods in detecting MET amplification, expression, and activation for targeted MET TKI treatment in non-small cell lung cancer patients

 

AMP

Multiple

Automated Analysis of Melanoma Gene Expression Patterns by Sequential Interrogation of Variable RNA Average Count-space.

 

AAPS

 

Applications of NanoString Technology in Clinical Trials

 

ASHG

Multiple

Nano-PipeRNA: A Modular Tool for Analysis of Complex NanoString Datasets

 

ISCB

AML

Concordance between Bone Marrow and Peripheral Blood Samples for Assessment of FLT3 Internal Tandem Duplication (ITD) Mutations: Data from Patients Screened for Participation in Quantum-R, a Global, Randomized, Open-Label, Phase 3 Study Examining the Effect of Quizartinib Monotherapy Vs Salvage Chemotherapy on Overall Survival in Patients with FLT3- ITD - Mutated AML Who Are Refractory to or Have Relapsed after First-Line Therapy

 

ASH

Heme & Solid

qPCR Methods for Characterizing Cellular Kinetics

 

AAPS

Heme & Solid

Transforming Oncology Drug Clinical Development by Next Generation Sequencing Testing

 

International Precision Medicine Convention

Heme & Solid

Transforming Oncology Drug Clinical Development by Next Generation Sequencing Testing

 

AAPS

 

Analytical Evaluation and Applications of the nCounter Vantage™ RNA:Protein Immune Cell Profiling Panel

 

AMP

 

Next Generation Sequencing (NGS) Evaluation of CYP11B1 and CYP11B2 Single Nucleotide Variants (SNP) for a Correlation in Hypertension and Cushing Syndrome

 

ASHG

 

Development of Bioassays for Checkpoint Immunotherapy. 

 

LSCO

 

Biomarkers to Support the Development and Clinical Application of Immunotherapy Combinations

 

LSCO

 

Liquid Biopsy:  Non-Invasive Tumor Diagnosis and Treatment Monitoring

 

SABPA-MDD

 

Promises and Challenges of Using Digital PCR

 

LSCO

 

Copy Number Variations:  Digital PCR, Nanostring, and Next Generation Sequencing.  

 

Digital PCR Conference

 

Digital PCR for Patient Monitoring and Stratification in Clinical Trials.  

 

Tri-Con

 

Nanostring Assays for Patient Monitoring and Stratification in Clinical Trials. 
 

 

ASHG

 

Development of a nanostring copy number assay for a customized 55 gene panel using challenging formalin-fixed paraffin-embedded (FFPE) tumor samples. 

 

AACR