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