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.

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How one integrated laboratory test can detect both molecular and cytogenetic driving alterations across blood cancers

Resource type: Customer presentation

Technology: NGS

Application: Haematology

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Precise and accurate detection of mutations and copy number alterations in CLL using enrichment-based targeted NGS

Resource type: Scientific poster

Technology: NGS

Application: Haematology

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Evaluation of OGT’s SureSeq Myeloid Fusion Complete NGS Workflow Solution V2 for partner-agnostic fusion gene detection in acute leukaemias

Resource type: Scientific poster

Technology: NGS

Application: Haematology

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Integrated analysis of diverse genomic variants for the profiling of myeloid and lymphoid neoplasms by targeted hybrid capture next-generation sequencing

Resource type: Scientific poster

Technology: NGS

Application: Haematology

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Sequencing depth vs. sequencing batching

Resource type: Article

Technology: NGS

Application: Haematology

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Optimising CD138 cell selection for Multiple Myeloma FISH

Resource type: Article

Technology: FISH

Application: Haematology

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The value of MRD assessment in AML

Resource type: Article

Technology: NGS

Application: Haematology

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The future of chronic lymphocytic leukaemia (CLL) genomics?

Resource type: Article

Technology: NGS

Application: Haematology

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Target capture NGS for use in molecular-based research of myeloid MRD

Resource type: Scientific poster

Technology: NGS

Application: Haematology

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Capturing fusions in haematological malignancies through targeted RNAseq

Resource type: Scientific poster

Technology: NGS

Application: Haematology

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Sequencing depth vs. VAF sensitivity

Resource type: Article

Technology: NGS

Application: Haematology

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Optimise your FISH assay: Simple fixes for reducing high background signal

Resource type: Article

Technology: FISH

Application: Haematology

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FISH, NGS and array resources

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

Filter by:

94 results

How one integrated laboratory test can detect both molecular and cytogenetic driving alterations across blood cancers

Precise and accurate detection of mutations and copy number alterations in CLL using enrichment-based targeted NGS

Evaluation of OGT’s SureSeq Myeloid Fusion Complete NGS Workflow Solution V2 for partner-agnostic fusion gene detection in acute leukaemias

Integrated analysis of diverse genomic variants for the profiling of myeloid and lymphoid neoplasms by targeted hybrid capture next-generation sequencing

Sequencing depth vs. sequencing batching

Optimising CD138 cell selection for Multiple Myeloma FISH

The value of MRD assessment in AML

The future of chronic lymphocytic leukaemia (CLL) genomics?

Target capture NGS for use in molecular-based research of myeloid MRD

Capturing fusions in haematological malignancies through targeted RNAseq

Sequencing depth vs. VAF sensitivity

Optimise your FISH assay: Simple fixes for reducing high background signal

Don't shoulder your lab's burden alone