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Genetic programming neural networks: A powerful bioinformatics tool for human genetics

, , , , and . Applied Soft Computing, 7 (1): 471--479 (January 2007)
DOI: doi:10.1016/j.asoc.2006.01.013

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Multivariate Analysis of Regulatory Snps: Empowering Personal Genomics by Considering Cis-Epistasis and Heterogeneity., and . Pacific Symposium on Biocomputing, page 276-287. World Scientific Publishing, (2011)Knowledge-Constrained K-Medoids Clustering of Regulatory Rare Alleles for Burden Tests., , and . EvoBIO, volume 7833 of Lecture Notes in Computer Science, page 35-42. Springer, (2013)Association Rule Discovery Has the Ability to Model Complex Genetic Effects., , and . CIDM, page 624-629. IEEE, (2007)Hadoop and PySpark for Reproducibility and Scalability of Genomic Sequencing Studies., , , , , , , and . PSB, page 523-534. (2020)Generating Linkage Disequilibrium Patterns in Data Simulations Using genomeSIMLA., , , , , , , and . EvoBIO, volume 4973 of Lecture Notes in Computer Science, page 24-35. Springer, (2008)Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia., , , , , , , , and . BMC Bioinform., 19 (1): 18:1-18:10 (2018)Local ancestry transitions modify snp-trait associations., , , and . PSB, page 424-435. (2018)Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record., , , , and . CRI, AMIA, (2017)Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry., , , , , , , and . BioData Min., (2015)Establishing the Need for Personalized Medicine: Simvastatin Exposure Among a SLCO1B1 Variant Population., , , and . AMIA, AMIA, (2013)