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Comprehensive panel detects single-nucleotide variants (SNVs), amplifications, and fusions that contribute to solid tumor progression.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
Access a variety of NGS and array educational resources for clinical cancer research, including assorted videos and scientific papers.
Dr. Rahman reviews characteristics of known cancer predisposition genes and the potential prospects of future discoveries.
Nature Genetics presents the iCOGS Focus, which comprises a collection of 13 papers by the COGS Consortium.
Sequencing melanoma-prone family identified disease-segregating germline mutation in promoter of telomerase reverse transcriptase gene.
Jackson et al. demonstrate the use of high-density arrays to identify copy number changes in pediatric rhabdoid tumors.
Ho et al. identify 3 distinct subtypes of orbital meningioma via genetic profiling with microarrays.
Harada et al. use arrays to detect deletions and copy-neutral loss of heterozygosity.
Dr. Riazalhosseini at McGill University preserves the integrity of FFPE samples to analyze disease-causing mutations.
Dr. Navin at MD Anderson Cancer Center uses single-cell sequencing to analyze heterogeneity in tumor subpopulations.
Dr. Trilochan Sahoo, Director of Cytogenetics at Combimatrix, discusses array-based cytogenetic analysis for cancer.
Scientists at Cancer Genetics, Inc discuss how targeted NGS helps identify myeloid-related genes with greater sensitivity.
Deep analysis of exosomal DNA found in the blood of pancreatic cancer subjects offers insight into the potential of liquid biopsies.
A new enrichment-based cancer research assay interrogates both DNA and RNA, detecting small variants, gene amplifications, gene fusions, and splice variants.
Dr. Fellowes at Peter MacCallum Cancer Centre discusses how his team uses Illumina technology.
Nicholas J. Schork, PhD speaks about whole human genome variation, cancer driver mutations, and clinical sequencing.
Luis Diaz, MD at Johns Hopkins School of Medicine discusses using NGS to analyze ovarian and endometrial cancers.
Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.
Kenneth Bloom, MD, FCAP, Chief Medical Officer at Clarient (GE Healthcare) discusses the practical aspects of applying NGS in clinical research.
Visit our Medical Genetics website to download an introduction to NGS technology and applications for molecular pathologists.
View educational resources from recognized oncology experts and regulatory bodies about applying NGS in a clinical research setting.
View educational resources from recognized oncology experts and regulatory bodies about applying NGS in a clinical setting.
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