Celina Whalley

Let’s Go Dotty for Lynch Syndrome – bridging the gap between testing and diagnosis

By Celina Whalley / March 22, 2024 / Comments Off on Let’s Go Dotty for Lynch Syndrome – bridging the gap between testing and diagnosis

Supporting Let’s Go Dotty: Lynch Syndrome Awareness Day March 22nd, 2024. A one-test NGS solution for Lynch Syndrome screening.

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Screening for rare disease with next generation sequencing

By Celina Whalley / February 24, 2024 / Comments Off on Screening for rare disease with next generation sequencing

Screening for rare disease with a clinically enhanced exome panel enabling CNV, SNV and INDEL calling in coding and non-coding regions.

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4 key factors influencing NGS custom panel design

By Celina Whalley / December 8, 2023 / Comments Off on 4 key factors influencing NGS custom panel design

Factors to take into account when planning custom panel design; target regions, coverage v depth, experimental noise and validation.

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FFPE, cfDNA and gDNA: The guide to DNA sample types used in next generation sequencing

By Celina Whalley / December 7, 2023 / Comments Off on FFPE, cfDNA and gDNA: The guide to DNA sample types used in next generation sequencing

Review of DNA types used in next generation sequencing (NGS), their quality characteristics and influence on choice of NGS assay.

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