Resources for clinical cancer researchers

Clinical Cancer Research Resources

Access a variety of NGS and array educational resources for clinical cancer research, including assorted videos and scientific papers.

 

Oncology
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Realizing the Promise of Cancer Predisposition Genes

Dr. Rahman reviews characteristics of known cancer predisposition genes and the potential prospects of future discoveries.

Open Nature.com
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A Collaborative Model for Oncology Studies

Nature Genetics presents the iCOGS Focus, which comprises a collection of 13 papers by the COGS Consortium.

Open Nature.com
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Sequencing Identifies TERT Promoter Germline Mutations

Sequencing melanoma-prone family identified disease-segregating germline mutation in promoter of telomerase reverse transcriptase gene.

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Array-Based Analysis of Chromosomal Alterations

Jackson et al. demonstrate the use of high-density arrays to identify copy number changes in pediatric rhabdoid tumors.

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Cancer Cytogenetics Study Identifies Meningioma Subtypes

Ho et al. identify 3 distinct subtypes of orbital meningioma via genetic profiling with microarrays.

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Using Arrays to Identify Genomic Changes in FFPE Gliomas

Harada et al. use arrays to detect deletions and copy-neutral loss of heterozygosity.

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Sequencing FFPE Samples to Identify Novel Biomarkers

Dr. Riazalhosseini at McGill University preserves the integrity of FFPE samples to analyze disease-causing mutations.

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Rare Tumor Cell Sequencing to Understand Cancer Evolution

Dr. Navin at MD Anderson Cancer Center uses single-cell sequencing to analyze heterogeneity in tumor subpopulations.

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Microarray-Based Cytogenetic Testing for Cancer

Dr. Trilochan Sahoo, Director of Cytogenetics at Combimatrix, discusses array-based cytogenetic analysis for cancer.

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NGS to Detect Blood Cancers
NGS to Detect Blood Cancers

Scientists at Cancer Genetics, Inc discuss how targeted NGS helps identify myeloid-related genes with greater sensitivity.

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Capturing Variant Data from the Blood
Capturing Variant Data from the Blood

Deep analysis of exosomal DNA found in the blood of pancreatic cancer subjects offers insight into the potential of liquid biopsies.

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Removing Cancer's Veil: TruSight Tumor 170

A new enrichment-based cancer research assay interrogates both DNA and RNA, detecting small variants, gene amplifications, gene fusions, and splice variants.

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How NGS is Revolutionizing Clinical Cancer Research

Dr. Fellowes at Peter MacCallum Cancer Centre discusses how his team uses Illumina technology.

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WGS to Identify Pathogenic Cancer Mutations

Nicholas J. Schork, PhD speaks about whole human genome variation, cancer driver mutations, and clinical sequencing.

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Using NGS to Analyze Ovarian and Endometrial Cancers

Luis Diaz, MD at Johns Hopkins School of Medicine discusses using NGS to analyze ovarian and endometrial cancers.

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Easy NGS Adoption for Tumor Profiling

Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.

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NGS in Clinical Research

Kenneth Bloom, MD, FCAP, Chief Medical Officer at Clarient (GE Healthcare) discusses the practical aspects of applying NGS in clinical research.

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Introduction to NGS for Pathologists

Visit our Medical Genetics website to download an introduction to NGS technology and applications for molecular pathologists.

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Resources for Applying NGS in a Clinical Research Setting

View educational resources from recognized oncology experts and regulatory bodies about applying NGS in a clinical research setting.

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Resources for Applying NGS in a Clinical Setting
Resources for Applying NGS in a Clinical Setting

View educational resources from recognized oncology experts and regulatory bodies about applying NGS in a clinical setting.

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