dbCPM: a manually curated database for exploring the cancer passenger mutations
暂无分享,去创建一个
Junfeng Xia | Zhenyu Yue | Le Zhao | Junfeng Xia | Zhenyu Yue | Le Zhao
[1] Cathy H. Wu,et al. UniProt: the Universal Protein knowledgebase , 2004, Nucleic Acids Res..
[2] T. Hubbard,et al. A census of human cancer genes , 2004, Nature Reviews Cancer.
[3] Zechen Chong,et al. TransVar: a multilevel variant annotator for precision genomics , 2015, Nature Methods.
[4] M. King,et al. Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2 , 2003, Science.
[5] Gang Feng,et al. Disease Ontology: a backbone for disease semantic integration , 2011, Nucleic Acids Res..
[6] Steven J. M. Jones,et al. Comprehensive Characterization of Cancer Driver Genes and Mutations , 2018, Cell.
[7] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[8] D. Haussler,et al. Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes. , 2005, Genome research.
[9] W. Miller,et al. PhenCode: connecting ENCODE data with mutations and phenotype , 2007, Human mutation.
[10] Tugba G. Kucukkal,et al. Structural and physico-chemical effects of disease and non-disease nsSNPs on proteins. , 2015, Current opinion in structural biology.
[11] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[12] M. Stratton,et al. The cancer genome , 2009, Nature.
[13] Ramaswamy K. Iyer,et al. Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing , 2014, PloS one.
[14] Joshua F. McMichael,et al. DoCM: a database of curated mutations in cancer , 2016, Nature Methods.
[15] Ken Chen,et al. Systematic Functional Annotation of Somatic Mutations in Cancer. , 2018, Cancer cell.
[16] Alessandra Viel,et al. Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2 , 1999, European Journal of Human Genetics.
[17] S. Henikoff,et al. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm , 2009, Nature Protocols.
[18] C. Orengo,et al. Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical use , 2016, Oncotarget.
[19] A. Jemal,et al. Cancer statistics, 2018 , 2018, CA: a cancer journal for clinicians.
[20] James G. Lyons,et al. Improving prediction of secondary structure, local backbone angles, and solvent accessible surface area of proteins by iterative deep learning , 2015, Scientific Reports.
[21] Robert D. Finn,et al. The Pfam protein families database: towards a more sustainable future , 2015, Nucleic Acids Res..
[22] Johannes H. Hegemann,et al. Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies , 2011, Familial Cancer.
[23] Eliot Y. Zhu,et al. Cancer Driver Log (CanDL): Catalog of Potentially Actionable Cancer Mutations. , 2015, The Journal of molecular diagnostics : JMD.
[24] Tom R. Gaunt,et al. Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models , 2012, Human mutation.
[25] Walter F. Bodmer,et al. Genotyping Possible Polymorphic Variants of Human Mismatch Repair Genes in Healthy Korean Individuals and Sporadic Colorectal Cancer Patients , 2004, Familial Cancer.
[26] Ricardo Villamarín-Salomón,et al. ClinVar: public archive of interpretations of clinically relevant variants , 2015, Nucleic Acids Res..
[27] Avni Santani,et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification , 2015, Genome research.
[28] Mikio Kan,et al. Constitutive activating mutation of the FGFR3b in oral squamous cell carcinomas , 2005, International journal of cancer.
[29] Moriah H Nissan,et al. OncoKB: A Precision Oncology Knowledge Base. , 2017, JCO precision oncology.
[30] Leyla Isik,et al. Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. , 2009, Cancer research.
[31] Jerven T. Bolleman,et al. Genetic Variations and Diseases in UniProtKB/Swiss-Prot: The Ins and Outs of Expert Manual Curation , 2014, Human mutation.
[32] Mauno Vihinen,et al. VariSNP, A Benchmark Database for Variations From dbSNP , 2015, Human mutation.
[33] D. Haber,et al. Cancer: Drivers and passengers , 2007, Nature.
[34] Charles Swanton,et al. My Cancer Genome: a unified genomics and clinical trial portal , 2012 .
[35] Data production leads,et al. An integrated encyclopedia of DNA elements in the human genome , 2012 .
[36] G. Mills,et al. CanDrA: Cancer-Specific Driver Missense Mutation Annotation with Optimized Features , 2013, PloS one.
[37] Larry N. Singh,et al. Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes. , 2012, American journal of human genetics.
[38] A. Gonzalez-Perez,et al. Improving the prediction of the functional impact of cancer mutations by baseline tolerance transformation , 2012, Genome Medicine.
[39] Li Ding,et al. Activating HER2 mutations in HER2 gene amplification negative breast cancer. , 2013, Cancer discovery.
[40] C. Sander,et al. Predicting the functional impact of protein mutations: application to cancer genomics , 2011, Nucleic acids research.
[41] Raymond Dalgleish,et al. HGVS Recommendations for the Description of Sequence Variants: 2016 Update , 2016, Human mutation.
[42] P. Bork,et al. A method and server for predicting damaging missense mutations , 2010, Nature Methods.
[43] Qiong He,et al. The MLH1 2101C>A (Q701K) variant increases the risk of gastric cancer in Chinese males , 2011, BMC gastroenterology.
[44] M. Vihinen. How to evaluate performance of prediction methods? Measures and their interpretation in variation effect analysis , 2012, BMC Genomics.
[45] Tom R. Gaunt,et al. CScape: a tool for predicting oncogenic single-point mutations in the cancer genome , 2017, Scientific Reports.