We are aware of current issues with the ONS login and account creation. At this time, account creation is unavailable. Users who already have an account with ONS should clear their device history/cache before attempting to log in. Thank you.
cancel
Genomics Taxonomy References
- BEST (Biomarkers, EndpointS, and other Tools) Resource https://www.ncbi.nlm.nih.gov/books/NBK338448/#IX-S
- NCI Dictionary of Cancer Terms https://www.cancer.gov/publications/dictionaries/cancer-terms
- NCI Dictionary of Genetic Terms https://www.cancer.gov/publications/dictionaries/genetics-dictionary
- NHGRI Talking Glossary Dictionary of Terms https://www.genome.gov//genetics-glossary/c#glossary
- PDQ Cancer Genetics Overview. https://www.cancer.gov/about-cancer/causes-prevention/genetics/overview-pdq#_146
- PharmGKB https://www.pharmgkb.org/
- Presidential Commission for the Study of Bioethical Issues (2013). ANTICIPATE and COMMUNICATE Ethical Management of Incidental and Secondary Findings in the Clinical, Research, and Direct-to-Consumer Contexts. https://bioethicsarchive.georgetown.edu/pcsbi/sites/default/files/FINALAnticipateCommunicate_PCSBI_0.pdf
- Richards et al. (2015). Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine.
- Stratton, M., Campbell, P., & Futreal, P. (2009). The cancer genome. Nature, 9;458, 719-724. doi: 10.1038/nature07943.
- Sukhai, M., Craddock, K., Thomas, M. et al. A classification system for clinical relevance of somatic variants identified in molecular profiling of cancer. Genet Med 18, 128–136 (2016). https://doi.org/10.1038/gim.2015.47
- National Human Genome Research Institute. (2020). Cost of Genome. https://www.genome.gov/about-genomics/fact-sheets/DNA-Sequencing-Costs-Data Accessed 5/27/2020.
- Richards, S., Aziz, N., Bale, S., et al. (2015). Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med, 17(5), 405-424. doi:10.1038/gim.2015.30
- PDQ Genetics of Breast and Gynecologic Cancers. (2020). https://www.cancer.gov/types/breast/hp/breast-ovarian-genetics-pdq#_110_toc
- PDQ Genetics of Colorectal Cancer. (2020). https://www.cancer.gov/types/colorectal/hp/colorectal-genetics-pdq#_2986_toc
- National Human Genome Research Institute Chromosome Abnormality Fact Sheet. (2020). https://www.genome.gov/about-genomics/fact-sheets/Chromosome-Abnormalities-Fact-Sheet
- Li¸M., Datto, M., Duncavage, E.J., et al. (2016). Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists. The Journal of Molecular Diagnostics, 19, 4e23. DOI: https://doi.org/10.1016/j.jmoldx.2016.10.002
- Ulaner, G. A., Riedl, C. C., Dickler, M. N., Jhaveri, K., Pandit-Taskar, N., & Weber, W. (2016). Molecular Imaging of Biomarkers in Breast Cancer. Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 57 Suppl 1(Suppl 1), 53S–9S. https://doi.org/10.2967/jnumed.115.157909
- Mandelker, D. and O. Ceyhan-Birsoy, Evolving Significance of Tumor-Normal Sequencing in Cancer Care. Trends Cancer, 2020. 6(1): p. 31-39. PMID: 31952779
- Strom S. P. (2016). Current practices and guidelines for clinical next-generation sequencing oncology testing. Cancer biology & medicine, 13(1), 3–11. https://pubmed.ncbi.nlm.nih.gov/27144058/
- Mandelker, D., & Ceyhan-Birsoy, O.). (2020). Evolving significance of tumor-normal sequencing in cancer care. Trends in Cancer, 6(1), 31-39. https://pubmed.ncbi.nlm.nih.gov/31952779/