Anil G. Jegga
Orcid: 0000-0002-4881-7752
According to our database1,
Anil G. Jegga
authored at least 30 papers
between 2005 and 2022.
Collaborative distances:
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Bibliography
2022
IEEE ACM Trans. Comput. Biol. Bioinform., 2022
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2022
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2022
2021
Secondary analysis of transcriptomes of SARS-CoV-2 infection models to characterize COVID-19.
Patterns, 2021
2020
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2020
A multi-context feature learning approach to identify disease-specific gene neighborhoods.
Proceedings of the BCB '20: 11th ACM International Conference on Bioinformatics, 2020
2014
ToppMiR: ranking microRNAs and their mRNA targets based on biological functions and context.
Nucleic Acids Res., 2014
2013
BMC Medical Informatics Decis. Mak., 2013
Large-scale evaluation of automated clinical note de-identification and its impact on information extraction.
J. Am. Medical Informatics Assoc., 2013
BMC Syst. Biol., 2013
Integrative genomics identifies candidate microRNAs for pathogenesis of experimental biliary atresia.
BMC Syst. Biol., 2013
Proceedings of the 13th IEEE International Conference on Data Mining Workshops, 2013
2012
A vertex similarity-based framework to discover and rank orphan disease-related genes.
BMC Syst. Biol., 2012
2011
Exploring Off-Targets and Off-Systems for Adverse Drug Reactions via Chemical-Protein Interactome - Clozapine-Induced Agranulocytosis as a Case Study.
PLoS Comput. Biol., 2011
2010
Stat. Anal. Data Min., 2010
ToppCluster: a multiple gene list feature analyzer for comparative enrichment clustering and network-based dissection of biological systems.
Nucleic Acids Res., 2010
Proceedings of the SIAM International Conference on Data Mining, 2010
2009
Nucleic Acids Res., 2009
Inferring novel disease indications for known drugs by semantically linking drug action and disease mechanism relationships.
BMC Bioinform., 2009
Correction: Disease candidate gene identification and prioritization using protein interaction networks.
BMC Bioinform., 2009
Disease candidate gene identification and prioritization using protein interaction networks.
BMC Bioinform., 2009
2008
Identifying disease-causal genes using Semantic Web-based representation of integrated genomic and phenomic knowledge.
J. Biomed. Informatics, 2008
2007
PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease.
Nucleic Acids Res., 2007
GenomeTrafac: a whole genome resource for the detection of transcription factor binding site clusters associated with conventional and microRNA encoding genes conserved between mouse and human gene orthologs.
Nucleic Acids Res., 2007
BMC Bioinform., 2007
Identifying Functional Binding Motifs of Tumor Protein p53 Using Support Vector Machines.
Proceedings of the Sixth International Conference on Machine Learning and Applications, 2007
2005
CisMols Analyzer: identification of compositionally similar <i>cis</i>-element clusters in ortholog conserved regions of coordinately expressed genes.
Nucleic Acids Res., 2005