Associated Papers
The evolutionary impact of childhood cancer on the human gene pool.
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Supplement: 41467_2024_45975_MOESM4_ESM.xlsx › Supplementary_Data_5
Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach.
Bhai P et al.
Frontiers in Genetics, 2021
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Supplement: Data_Sheet_1.zip › Supplementary_files › Supplementary_Table_S4.xlsx › Variant_summary
TAPES: A tool for assessment and prioritisation in exome studies.
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Plos Computational Biology, 2019
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CharGer: clinical Characterization of Germline variants.
Scott AD et al.
Bioinformatics (oxford, England), 2019
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