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NeoGenomics to Present New Data at AMP 2024, Highlighting the Impact of ctDNA and NGS for Advancing Cancer Diagnostics and Personalized Treatment

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NeoGenomics (NASDAQ: NEO) will present four abstracts at the AMP 2024 Annual Meeting & Expo in Vancouver, showcasing advancements in cancer diagnostics through ctDNA and next-generation sequencing (NGS). The presentations include research on: the G4 sequencing platform for gene fusion detection, TSO500 ctDNA v2 assay performance, enhanced workflow for Neo Comprehensive™ tumor profiling, and HPV subtyping using whole transcriptome sequencing.

The company will also host a workshop on November 20 focusing on comprehensive genomic profiling for myeloid neoplasms. These presentations demonstrate NeoGenomics' commitment to improving cancer care through precision medicine and advanced testing methodologies.

NeoGenomics (NASDAQ: NEO) presenterà quattro abstract durante il AMP 2024 Annual Meeting & Expo a Vancouver, mostrando i progressi nella diagnosi del cancro attraverso il ctDNA e il sequenziamento di nuova generazione (NGS). Le presentazioni includono ricerche sulla piattaforma di sequenziamento G4 per la rilevazione delle fusioni geniche, le prestazioni dell'assay TSO500 ctDNA v2, un flusso di lavoro migliorato per il profilo tumorale Neo Comprehensive™ e la suddivisione dell'HPV tramite sequenziamento dell'intero trascrittoma.

L'azienda ospiterà anche un workshop il 20 novembre incentrato sul profilo genomico completo per le neoplasie mieloidi. Queste presentazioni dimostrano l'impegno di NeoGenomics nel migliorare l'assistenza al cancro attraverso la medicina di precisione e metodologie di test avanzate.

NeoGenomics (NASDAQ: NEO) presentará cuatro resúmenes en el AMP 2024 Annual Meeting & Expo en Vancouver, mostrando avances en el diagnóstico del cáncer a través de ctDNA y secuenciación de nueva generación (NGS). Las presentaciones incluyen investigaciones sobre: la plataforma de secuenciación G4 para la detección de fusiones génicas, el desempeño del ensayo TSO500 ctDNA v2, un flujo de trabajo mejorado para el perfil tumoral Neo Comprehensive™ y la subtipificación de HPV mediante secuenciación del transcriptoma completo.

La empresa también organizará un taller el 20 de noviembre centrado en el perfil genómico integral para neoplasias mieloides. Estas presentaciones demuestran el compromiso de NeoGenomics para mejorar la atención del cáncer a través de la medicina de precisión y metodologías de prueba avanzadas.

NeoGenomics (NASDAQ: NEO)는 밴쿠버에서 열리는 AMP 2024 Annual Meeting & Expo에서 ctDNA 및 차세대 시퀀싱(NGS)을 통한 암 진단의 발전을 보여주는 네 개의 초록을 발표할 것입니다. 발표 내용에는 유전자 융합 감지를 위한 G4 시퀀싱 플랫폼, TSO500 ctDNA v2 분석 성능, Neo Comprehensive™ 종양 프로파일링을 위한 향상된 작업 흐름, 전체 전사체 시퀀싱을 통한 HPV 아형 분류에 대한 연구가 포함됩니다.

회사는 또한 11월 20일 골수 신생물에 대한 포괄적인 유전체 프로파일링에 중점을 둔 워크숍을 개최할 것입니다. 이러한 발표는 정밀 의학 및 고급 검사 방법론을 통해 암 치료 향상에 대한 NeoGenomics의 헌신을 보여줍니다.

NeoGenomics (NASDAQ: NEO) présentera quatre résumés lors du AMP 2024 Annual Meeting & Expo à Vancouver, mettant en avant les avancées dans le diagnostic du cancer grâce au ctDNA et au séquençage de nouvelle génération (NGS). Les présentations incluent des recherches sur : la plateforme de séquençage G4 pour la détection des fusions géniques, la performance du test TSO500 ctDNA v2, un flux de travail amélioré pour le profilage tumoral Neo Comprehensive™ et la typification de l'HPV à l'aide du séquençage de l'ensemble du transcriptome.

L'entreprise animera également un atelier le 20 novembre centré sur le profilage génomique complet pour les néoplasies myéloïdes. Ces présentations démontrent l'engagement de NeoGenomics à améliorer les soins contre le cancer grâce à la médecine de précision et à des méthodologies de test avancées.

NeoGenomics (NASDAQ: NEO) wird auf dem AMP 2024 Annual Meeting & Expo in Vancouver vier Abstracts präsentieren, die Fortschritte in der Krebsdiagnose durch ctDNA und Next-Generation Sequencing (NGS) zeigen. Die Präsentationen beinhalten Forschungen zur G4-Sequenzierungsplattform zur Erkennung von Genfusionen, zur Leistung des TSO500 ctDNA v2 Assays, zu einem verbesserten Arbeitsablauf für das Neo Comprehensive™ Tumorprofiling und zur HPV-Subtypisierung mithilfe von Whole Transcriptome Sequencing.

Das Unternehmen wird auch am 20. November einen Workshop zur umfassenden genomischen Profilierung von myeloischen Neoplasien veranstalten. Diese Präsentationen zeigen das Engagement von NeoGenomics, die Krebsversorgung durch Präzisionsmedizin und fortschrittliche Testmethoden zu verbessern.

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FT. MYERS, Fla.--(BUSINESS WIRE)-- NeoGenomics, Inc. (NASDAQ: NEO), a leading oncology testing services company, will present four abstracts at the Association for Molecular Pathology (AMP) 2024 Annual Meeting & Expo in Vancouver, Canada, November 19-23 (booth #830). The research demonstrates how ctDNA and next-generation sequencing (NGS) can drive more personalized and accurate treatment options for cancer patients.

“Our presence at AMP 2024 underscores NeoGenomics’ dedication to advancing cancer care through ongoing research in precision medicine,” said Warren Stone, CCO of NeoGenomics. “By continuing to improve our methods and technologies, we aim to enhance outcomes and set new standards for oncology testing.”

NeoGenomics’ presentations include:

  • A Solid Tumor Gene Fusion Next-Generation Sequencing Assay on the G4 Sequencing Platform
    • Abstract #1874602: Friday, November 22 | 9:15-10:15 a.m. PST
    • The study highlights the G4 platform as a reliable and efficient alternative for clinical and genomic research applications, delivering high accuracy, speed, and flexibility.
  • Effect of Genomic DNA Contamination in Cell-Free DNA on the Assay Performance of TSO500 ctDNA v2
    • Abstract #1874288: Friday, November 22 | 9:15-10:15 a.m. PST
    • The data shows that the TSO500 ctDNA v2 assay maintains high sensitivity for detecting tumor mutations, even with significant genomic DNA contamination, ensuring reliable results for cancer profiling through liquid biopsy.
  • An Enhanced Workflow for the Neo Comprehensive™ Solid Tumor Genome Profiling Assay: Comparison for Tecan Qubit vs KAPA Library Quantification
    • Abstract #1874050: Friday, November 22 | 9:15-10:15 a.m. PST
    • The study validates an improved workflow for the Neo Comprehensive™ solid tumor genome profiling NGS panel, offering significant time savings and reducing errors while maintaining equivalent accuracy and performance.
  • Human Papillomavirus Subtyping Using Whole Transcriptome Sequencing
    • Abstract #1874277: Saturday, November 23 | 9:15-10:15 a.m. PST
    • The data demonstrates that NeoGenomics’ bioinformatics pipeline can identify and classify HPV cases into high and low-risk subtypes with similar performance to more traditional methods, delivering added value and potential cost savings for patients.

NeoGenomics will also host a corporate workshop on November 20, 8-8:50 a.m. PST, titled “Clinical Utility of Comprehensive Genomic Profiling (CGP) for Myeloid Neoplasms.” The session will highlight the utility of myeloid comprehensive genomic profiling across a broad spectrum of categories, including acute myeloid leukemia, where rapid genomic testing may lead to improved patient outcomes.

For more details on NeoGenomics’ presentations, visit the AMP website.

About NeoGenomics, Inc.

NeoGenomics, Inc. specializes in cancer genetics testing and information services, providing one of the most comprehensive oncology-focused testing menus for physicians to help them diagnose and treat cancer. The Company's Advanced Diagnostic Division also serves pharmaceutical clients in clinical trials and drug development.

Headquartered in Fort Myers, FL, NeoGenomics operates CAP accredited and CLIA certified laboratories for full-service sample processing in Fort Myers, Florida; Aliso Viejo and San Diego, California; Research Triangle Park, North Carolina; and Houston, Texas; and a CAP accredited full-service, sample-processing laboratory in Cambridge, United Kingdom. NeoGenomics also has several, small, non-processing laboratory locations across the United States for providing analysis services. NeoGenomics serves the needs of pathologists, oncologists, academic centers, hospital systems, pharmaceutical firms, integrated service delivery networks, and managed care organizations throughout the United States, and pharmaceutical firms in Europe and Asia.

Forward-Looking Statements

This press release includes forward-looking statements. These forward-looking statements generally can be identified by the use of words such as “anticipate,” “expect,” “plan,” “could,” “would,” “may,” “will,” “believe,” “estimate,” “forecast,” “goal,” “project,” “guidance,” “plan,” “potential” and other words of similar meaning, although not all forward-looking statements include these words. This press release includes forward-looking statements. These forward-looking statements address various matters, including statements regarding improving operational efficiency, returning to profitable growth and its ongoing executive recruitment process. Each forward-looking statement contained in this press release is subject to a number of risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statement. Applicable risks and uncertainties include, among others, the Company's ability to identify and implement appropriate financial and operational initiatives to improve performance, to identify and recruit executive candidates, to continue gaining new customers, offer new types of tests, integrate its acquisitions and otherwise implement its business plan, and the risks identified under the heading "Risk Factors" contained in the Company's Annual Report on Form 10-K, Quarterly Reports on Form 10-Q and the Company's other filings with the Securities and Exchange Commission.

We caution investors not to place undue reliance on the forward-looking statements contained in this press release. You are encouraged to read our filings with the SEC, available at www.sec.gov, for a discussion of these and other risks and uncertainties. The forward-looking statements in this press release speak only as of the date of this document (unless another date is indicated), and we undertake no obligation to update or revise any of these statements. Our business is subject to substantial risks and uncertainties, including those referenced above. Investors, potential investors, and others should give careful consideration to these risks and uncertainties.

Investor Contact

Kendra Sweeney

kendra.sweeney@neogenomics.com

Media Contact

Andrea Sampson

asampson@sampsonprgroup.com

Source: NeoGenomics, Inc.

FAQ

What research will NeoGenomics (NEO) present at AMP 2024?

NeoGenomics will present four abstracts covering G4 platform sequencing, TSO500 ctDNA v2 assay performance, Neo Comprehensive™ tumor profiling workflow, and HPV subtyping using whole transcriptome sequencing.

When and where is NeoGenomics (NEO) presenting at AMP 2024?

NeoGenomics will present at the AMP 2024 Annual Meeting & Expo in Vancouver, Canada, from November 19-23, at booth #830.

What is the topic of NeoGenomics' (NEO) corporate workshop at AMP 2024?

NeoGenomics will host a workshop on November 20 titled 'Clinical Utility of Comprehensive Genomic Profiling (CGP) for Myeloid Neoplasms,' focusing on genomic profiling applications in myeloid conditions.

What did the TSO500 ctDNA v2 assay study by NeoGenomics (NEO) reveal?

The study showed that the TSO500 ctDNA v2 assay maintains high sensitivity in detecting tumor mutations even with significant genomic DNA contamination, ensuring reliable liquid biopsy results.

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