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Jack Reilly

London Health Sciences Centre

4

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109

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Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach.

2021 Frontiers in Genetics
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EpiSigns: DNA Methylation Signatures in Mendelian Neurodevelopmental Disorders as a Diagnostic Link Between a Genotype and Phenotype

2020
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Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels

2017 The Journal of Molecular Diagnostics
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Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis

2016 The Journal of Molecular Diagnostics
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