FISH, NGS and array resources

NGS advances: Efficient fusion event detection in haematological malignancy clinical research

Resource type: Application note

Technology: NGS

Application: Haematology

This study highlights the ability of the SureSeq™ Myeloid Fusion Panel to detect multiple fusions, identify breakpoints, and capture MECOM overexpression, so your lab can achieve higher efficiency sample classification with a single assay.

13 results

Beyond CNV: leveraging SNP microarrays in cancer

Resource type: Customer presentation

Technology: Arrays

Application: Solid tumour

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Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres

Resource type: White paper

Technology: Arrays

Application: Cytogenetics & rare disease

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The impact of microarray probe design on detecting copy number variants at exon-resolution

Resource type: Application note

Technology: Arrays

Application: Haematology

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The use of the InnoScan 710 scanner and Mapix software with CytoSure microarrays

Resource type: Application note

Technology: Arrays

Application: Haematology

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The whole exome: Completing the genomic picture using exon-targeted aCGH

Resource type: Customer presentation

Technology: Arrays

Application: Cytogenetics & rare disease

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Superior detection of chromosomal aberrations using the latest generation of exon-focused constitutional arrays

Resource type: White paper

Technology: Arrays

Application: Cytogenetics & rare disease

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Adoption of the CytoSure Constitutional v3 microarray for increased detection of disease-relevant variants

Resource type: White paper

Technology: Arrays

Application: Cytogenetics & rare disease

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Advancing genomic interpretation: combining NGS and microarrays

Resource type: Customer presentation

Technology: Arrays

Application: Cytogenetics & rare disease

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Validation of the CytoSure Constitutional v3 microarrays in prenatal and postnatal analysis

Resource type: Customer presentation

Technology: Arrays

Application: Cytogenetics & rare disease

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Implementation of the CytoSure Constitutional v3 microarray in the UK NHS

Resource type: Customer presentation

Technology: Arrays

Application: Cytogenetics & rare disease

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Customisable, exon-focused aCGH microarrays complement NGS for additional insights into genetic disorders

Resource type: Customer presentation

Technology: Arrays

Application: Cytogenetics & rare disease

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Examining the medical exome

Resource type: White paper

Technology: Arrays

Application: Cytogenetics & rare disease

View resource

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FISH, NGS and array resources

NGS advances: Efficient fusion event detection in haematological malignancy clinical research

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13 results

Beyond CNV: leveraging SNP microarrays in cancer

Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres

The impact of microarray probe design on detecting copy number variants at exon-resolution

The use of the InnoScan 710 scanner and Mapix software with CytoSure microarrays

The whole exome: Completing the genomic picture using exon-targeted aCGH

Superior detection of chromosomal aberrations using the latest generation of exon-focused constitutional arrays

Adoption of the CytoSure Constitutional v3 microarray for increased detection of disease-relevant variants

Advancing genomic interpretation: combining NGS and microarrays

Validation of the CytoSure Constitutional v3 microarrays in prenatal and postnatal analysis

Implementation of the CytoSure Constitutional v3 microarray in the UK NHS

Customisable, exon-focused aCGH microarrays complement NGS for additional insights into genetic disorders

Examining the medical exome

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