Literature

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

Greater confidence in calling low-frequency variants – from as little as 10ng of severely formalin-compromised DNA

In this study, carried out in collaboration with Horizon Discovery, formalin-compromised DNA (fcDNA) samples of differing severity were repaired with the SureSeq™ FFPE repair mix and sequenced using a SureSeq custom hybridisation-based panel.

Type: Application note