Comparison of open-access databases for clinical variant interpretation in cancer: A case study of MDS/AML

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Abstract

Background: Recently, guidelines for variant interpretation in cancer have been established. However, these guidelines do not mention which databases are most suited to performing this task. Materials and Methods: We give an overview of existing databases and evaluate their benefit in practical application. We compared three meta-databases and 12 databases for a dataset of patients with myelodysplastic syndrome or acute myeloid leukemia. Results: Clinical implications were found for 13% of all variants. One-third of variants with therapeutic implications were uniquely contained in one database. The VICC meta-database was the most extensive source of information, featuring 92% of variants with a drug association. However, a comparison of meta-databases and original sources indicated that some variants are missing in those meta-databases. Conclusion: Public databases provide decision support for interpreting variants but there is still need for manual curation. Meta-databases facilitate the use of multiple resources but should be interpreted with caution.

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Banck, H., Dugas, M., Müller-Tidow, C., & Sandmann, S. (2021). Comparison of open-access databases for clinical variant interpretation in cancer: A case study of MDS/AML. Cancer Genomics and Proteomics, 18(2), 157–166. https://doi.org/10.21873/CGP.20250

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