Associated Papers
Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach.
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Frontiers in Genetics, 2021
34326862 (PubMed )
Supplement: Data_Sheet_1.zip › Supplementary_files › Supplementary_Table_S4.xlsx › Variant_summary
Benchmarking mutation effect prediction algorithms using functionally validated cancer-related missense mutations.
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Supplement: 13059_2014_484_MOESM2_ESM.xlsx › Additional_file_2
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.
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Human Mutation, 2006
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