Dr Fortin will talk about transitioning from microarray to the SureSeq™ CLL + CNV NGS panel, and how the SureSeq CLL + CNV NGS Panel delivers a comprehensive genomic profile for each CLL sample using a single workflow, including trisomy 12, 11q, 13q and 17p deletions.
Dr. McCready will examine the utility of a CytoSure® Constitutional NGS panel to identify relevant variants in families with reduced penetrance or uncertain CNVs. Findings from this pilot cohort were compared to data from chromosome microarray analysis to evaluate feasibility of the NGS platform for copy number detection and its utility in identifying SNVs acting synergistically with CNVs to affect phenotype.
Dr. Tucker shares her experience of how OGT’s NGS panel, SureSeq™ CLL + CNV, has streamlined her laboratory workflow and enabled the detection of various aberrations in key genes implicated in CLL progression, including SNVs, indels, and CNVs. This alleviates the burden of running multiple assays and delivers comprehensive results with a single NGS analysis.
Dr. McCready will compare a hybridisation-based NGS panel versus single analyte and amplicon-based NGS assays for somatic mutation testing in myeloid malignancies, from her experience with OGT’s SureSeq myPanel™ Custom Myeloid - 49 gene plus panel.
Part I – Video illustrates the DNA fragmentation, end repair, and 3’ end A-tailing process in the Universal NGS Complete Workflow Solution.
Part II - Video illustrates the adapter ligation process and the purification of the ligated library in the Universal NGS Complete Workflow Solution.
Part III - Video illustrates the pre-capture PCR of the ligated library and its purification in the Universal NGS Complete Workflow Solution.
Part IV - Video illustrates the hybridisation process with design specific baits in the Universal NGS Complete Workflow Solution.
Part V – Video illustrates the post-capture PCR of the hybridised samples, and the final pooling for sequencing in the Universal NGS Complete Workflow Solution.
This video illustrates the key steps for enzymatic DNA fragmentation prior to library preparation using the SureSeq™ NGS Library Preparation Kit for solid tumour samples.
This video illustrates the key steps for AMPure® purification using the SureSeq™ NGS Library Preparation Kit for solid tumour samples.
This video illustrates the key steps for Dynabeads™ M270 Streptavidin magnetic bead preparation using the SureSeq™ NGS Library Preparation Kit for solid tumour samples.
This video illustrates the key steps for hybrid capture using the SureSeq™ NGS Library Preparation Kit for solid tumour samples.
This video illustrates the key steps for post-hybridisation bead washing using the SureSeq™ NGS Library Preparation Kit for solid tumour samples.
Learn about Interpret, OGT’s powerful and easy-to-use next generation sequencing analysis solution, designed to work seamlessly with SureSeq and CytoSure NGS panels.
Learn how easy it is to upload sample FASTQ files into OGT’s Interpret software and use them to create a batch for data analysis.
Learn how simply you can navigate round your analysis batch results and generate batch reports up front of variant analysis.
Learn how Interpret software creates easy to navigate displays of QC metrics to help users access the performance of their sequencing runs.
Find out how to view analysis results by variants and explore using this feature in the Interpret software.
Discover how to navigate and modify the Variant results page, selecting aberration types and customising data analysis displays and tables with the many options available.
Hear from our two AMP 2022 guest speakers about their experience utilising OGT’s SureSeq™ myeloid NGS research solutions in their genomic laboratories to detect key aberrations in myeloid malignancies, including CEBPA gene variants, FLT3-ITDS, and KMT2A-PTDs, among others.
Presented at GLGC 2022, hear how our customers Dr. Peter Sabatini and Dr. Graeme Quest streamlined their CLL research and utilised OGT’s SureSeq™ CLL + CNV NGS panel to detect CNVs in five chromosomal regions as well as SNVs and indels in key genes implicated in CLL.
Presented at the Festival of Genomics & Biodata 2022 conference, this presentation explores how OGT's SureSeq™ NGS panels allow accurate detection of low-frequency SNVs and indels, as well as structural aberrations such as ITDs, PTDs, CNVs, LOH and translocations.
Presented at the European Society of Human Genetics (ESHG) 2021 conference, discover how two scientists have streamlined their laboratory workflow using OGT’s NGS panels, allowing them to accurately detect a wide variety of genetic aberrations.
Presented at the Cancer Genomics Consortium (CGC) 2021 conference, Dr. Tracy Tucker shares her experience in utilising the SureSeq™ CLL + CNV NGS panel to transition her lab's CLL FISH analysis into the molecular biomarker era.
Presented at the American Cytogenetics Conference (ACC) 2021, this informative presentation explores transitioning from microarray to the SureSeq™ CLL + CNV NGS panel.
Presented at the American College of Medical Genetics and Genomics (ACMG) 2021 conference, learn from one of OGT’s customers how utilising CytoSure® Constitutional NGS panel assists in the detection of genetic modifiers in families with reduced penetrance or uncertain CNVs.
Presented at the Association for Molecular Pathology (AMP) 2020 conference, this 50-minute workshop highlights two scientists’ experiences using OGT’s NGS panels in their haematology workflows, delivering comprehensive results with a single NGS analysis.
In this webinar learn how the SureSeq™ CLL + CNV NGS Panel alleviates the burden of running multiple assays and streamlines your CLL research to deliver a comprehensive genomic profile for each CLL sample using a single NGS assay.
Watch this webinar and learn how the CytoSure® Constitutional NGS solution, which delivers CNV analysis with excellent concordance with the ‘gold standard’ method, aCGH, can make the transition from arrays to NGS as painless as possible.
