Literature
Improving experimental reproducibility through automated hybridisation-based NGS library preparation
In this application note, an Agilent Bravo A Automated Liquid Handling Platform was configured to run the SureSeq NGS library preparation protocol. The results demonstrate marked improvement not only in hands-on-time, but also a number of quality metrics
Type: Application note
SureSeq™ NGS Library Preparation Kit
Type: Product profile
SureSeq Library™ Preparation Handbook
Type: Handbook
SureSeq™ Quick Reference Guide – Good Quality DNA
Type: Guide
SureSeq myPanel™ NGS Custom Cancer Panels
Type: Product profile
Assessment of the performance of a hybridisation-based NGS enrichment panel with as little as 10 ng of severely formalin-compromised DNA
Presented at AMP 2018, this poster illustrates the excellent performance of a hybridisation-based NGS enrichment panel, in conjunction with an FFPE repair mix.
Type: Poster
Beyond FISH, SNVs and indels – improved resolution of translocation detection using next generation sequencing (NGS)
Presented at AMP 2018, this poster demonstrates how the superior uniformity of coverage of the hybridisation-based approach of the SureSeq™ protocol in combination with a SureSeq myPanel™ NGS Custom panel reliably detects somatic BCR-ABL1 translocations.
Type: Poster
Notes from the field: Cytocell Application Specialist, Gothami Fonseka
Type: Article
Notes from the Field: Cytocell Field Application Scientist, Ashley Hart
Type: Article
SureSeq™ Interpret Software
Type: Product profile
The Analysis of FFPE Samples by Next-Generation Sequencing (NGS) of Key Genes for Research into Breast and Ovarian Cancer
Presented at AMP Europe 2018, this poster illustrates the confident detection of germline and somatic variants in key cancer-related genes including BRCA1 and TP53.
Type: Poster
CytoSure™ Cancer +SNP Arrays
Type: Product profile
Interview: Erica Phillips, CG (ASCP), Clinical Cytogenetics Supervisor, Duke University Health System
Custom Genomic Research Solutions
OGT's custom NGS panels, custom arrays and custom FISH probes give researchers the ability to react to new discoveries, modify research workflows, and target specific regions in a fast-changing genomics research environment.
Type: Brochure
What’s wrong with my arrays?
Wet-lab processing is key to achieving the highest quality array data – find the solution to improve your data quality with our poster.
Type: Poster
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