Literature
Simultaneous Detection of Genetic and Copy-Number Variations in BRCA1/2 Genes
Presented at the AMP 2020 virtual meeting, this poster demonstrates the capability of the SureSeq™ Breast Cancer + CNV Panel in combination with Interpret software to detect germline and mosaic CNVs.
Type: Poster
OGT Product Catalog - USA and Canada
Including Cytocell® FISH probes for Constitutional Cytogenetics and Hematology/Pathology Cytogenetics, CytoSure™ NGS and Array Products for Cytogenetics and Rare Disease Research and SureSeq™ NGS Products for Hematology and Solid Tumor Cancer Research.
Type: Catalogue
SureSeq™ Breast Cancer + CNV Panel
Type: Product profile
SureSeq™ Pan-Myeloid Panel
Type: Product profile
OGT Product Catalogue
Including Cytocell® FISH Probes for Cancer and Inherited Genetic Disease, CytoSure™ NGS and Array Products for Cytogenetics and Rare Disease, and SureSeq™ NGS Products for Haematology and Solid Tumour Cancers.
Type: Catalogue
SureSeq myPanel™ NGS Custom AML Panels
Type: Product profile
Comparison of CytoSure™ Constitutional NGS with Microarrays for CNV detection
This technical note compares performance of CytoSure Constitutional NGS and a range of microarrays for 255 research samples processed in three independent laboratories and OGT.
Type: Application note
Interpret NGS Analysis Software
Type: Product profile
A next generation sequencing solution to detect copy number variants, single nucleotide variants and loss of heterozygosity in intellectual disability and developmental delay samples
Presented at ESHG Virtual 2020, this poster outlines the results from over 200 intellectual disability and developmental research samples to demonstrate the efficiency of the CNV, SNV and LOH detection.
Type: Poster
CytoSure™ Array Handbook (4x44k and 4x180k formats)
Type: Handbook
CytoSure™ Array Handbook (8x15k and 8x60k formats)
Type: Handbook
CytoSure™ HT Array Handbook (8x15k and 8x60k formats)
Type: Handbook
A New Next Generation Sequencing (NGS) Assay for Detecting the Aberrations in Intellectual Disability and Developmental Delay Samples
Presented at ACMG 2020, this poster demonstrates the capability of a novel NGS assay designed to analyse genetic aberrations, including CNVs, SNVs, Indels and LOH, in intellectual disability and developmental delay research samples.
Type: Poster
SureSeq™ Core MPN Panel
Type: Product profile
Interpret Quick-Start Guide
Download OGT's Interpret NGS analysis software quick-start guide, for use with SureSeq™ and CytoSure™ NGS panels.
Type: Guide
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