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
Deciphering DNA repair gene mutational landscape in uterine corpus endometrial carcinoma patients using next generation sequencing.
Lou J et al.
American Journal of Cancer Research, 2024
Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer.
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Frontiers in Genetics, 2023
36896237 (PubMed )
Supplement: Table1.xlsx › clinvar_breastcancer_allvariant
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
34326862 (PubMed )
Supplement: Data_Sheet_1.zip › Supplementary_files › Supplementary_Table_S4.xlsx › Every_test
TAPES: A tool for assessment and prioritisation in exome studies.
Xavier A et al.
Plos Computational Biology, 2019
31613886 (PubMed )
Supplement: pcbi.1007453.s005.zip › Initial_Benchmark › CharGer_and_Panel_Benchmark.xlsx › SupplTable2
CharGer: clinical Characterization of Germline variants.
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Bioinformatics (oxford, England), 2019
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Supplement: bioinformatics_35_5_865_s4.xlsx › SupplTable2
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