Anthony McGuigan
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View article: Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project
Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project Open
Background Whole-genome sequencing (WGS) projects for rare disease diagnosis typically yield a diagnostic rate of approximately 25-40%, dependent particularly on patient selection and the extent of prior genetic testing. The Scottish Genom…
View article: Multiplex analysis of intratumoural immune infiltrate and prognosis in patients with stage II–III colorectal cancer from the SCOT and QUASAR 2 trials: a retrospective analysis
Multiplex analysis of intratumoural immune infiltrate and prognosis in patients with stage II–III colorectal cancer from the SCOT and QUASAR 2 trials: a retrospective analysis Open
Medical Research Council, National Institute for Health Research, Cancer Research UK, Swedish Cancer Society, Roche, and Promedica Foundation.
View article: Accounting for intensity variation in image analysis of large‐scale multiplexed clinical trial datasets
Accounting for intensity variation in image analysis of large‐scale multiplexed clinical trial datasets Open
Multiplex immunofluorescence (mIF) imaging can provide comprehensive quantitative and spatial information for multiple immune markers for tumour immunoprofiling. However, application at scale to clinical trial samples sourced from multiple…
View article: Accounting for intensity variation in image analysis of large-scale multiplexed clinical trial datasets
Accounting for intensity variation in image analysis of large-scale multiplexed clinical trial datasets Open
Multiplex immunofluorescence (mIF) imaging can provide comprehensive quantitative and spatial information for multiple immune markers for tumour immunoprofiling. However, application at scale to clinical trial samples sourced from multiple…
View article: Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update
Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update Open