Subha Madhavan

According to our database1, Subha Madhavan authored at least 26 papers between 2011 and 2023.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of two.

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2023
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res., January, 2023

2022
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
J. Am. Medical Informatics Assoc., 2022

Exploring approaches for predictive cancer patient digital twins: Opportunities for collaboration and innovation.
Frontiers Digit. Health, 2022

2021
Recommendations for the safe, effective use of adaptive CDS in the US healthcare system: an AMIA position paper.
J. Am. Medical Informatics Assoc., 2021

Use of electronic health records to support a public health response to the COVID-19 pandemic in the United States: a perspective from 15 academic medical centers.
J. Am. Medical Informatics Assoc., 2021

2020
Identification of Patients with Immune-related Adverse Events from Clinical Notes using Machine Learning.
Proceedings of the 8th IEEE International Conference on Healthcare Informatics, 2020

Automated Identification of Patients with Immune-related Adverse Events from Clinical Notes using Machine Learning.
Proceedings of the AMIA 2020, 2020

Global research consortia and data harmonization projects drive the clinical interpretation of cancers.
Proceedings of the AMIA 2020, 2020

2019
SNP2SIM: a modular workflow for standardizing molecular simulation and functional analysis of protein variants.
BMC Bioinform., 2019

2018
POPSTR: Inference of Admixed Population Structure Based on Single-Nucleotide Polymorphisms and Copy Number Variations.
J. Comput. Biol., 2018

iTextMine: integrated text-mining system for large-scale knowledge extraction from the literature.
Database J. Biol. Databases Curation, 2018

ClinGen Cancer Somatic Working Group - Standardizing and democratizing access to cancer molecular diagnostic data to drive translational research.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

2017
UD_GU_BioTM at TREC 2017: Precision Medicine Track.
Proceedings of The Twenty-Sixth Text REtrieval Conference, 2017

Tumor Neoantigens Derived from RNA Sequencing Analysis.
Proceedings of the 8th ACM International Conference on Bioinformatics, 2017

2016
An informatics research agenda to support precision medicine: seven key areas.
J. Am. Medical Informatics Assoc., 2016

G-DOC <i>Plus</i> - an integrative bioinformatics platform for precision medicine.
BMC Bioinform., 2016

Translational Bioinformatics 101.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

2014
AISAIC: a software suite for accurate identification of significant aberrations in cancers.
Bioinform., 2014

2013
The CAM software for nonnegative blind source separation in R-Java.
J. Mach. Learn. Res., 2013

SNP2Structure: A public database for mapping and modeling nsSNPs on human protein structures.
Proceedings of the ACM Conference on Bioinformatics, 2013

In silico analysis of autoimmune diseases and genetic relationships to vaccination against infectious diseases.
Proceedings of the ACM Conference on Bioinformatics, 2013

An integrated pharmacogenomic analysis of doxorubicin response using genotype information on DMET genes.
Proceedings of the ACM Conference on Bioinformatics, 2013

2012
Informatics and data quality at collaborative multicenter Breast and Colon Cancer Family Registries.
J. Am. Medical Informatics Assoc., 2012

Accurate identification of significant aberrations in contaminated cancer genome.
Proceedings of the Proceedings 2012 IEEE International Workshop on Genomic Signal Processing and Statistics, 2012

2011
DDN: a caBIG<sup>®</sup> analytical tool for differential network analysis.
Bioinform., 2011

PUGSVM: a caBIG<sup>TM</sup> analytical tool for multiclass gene selection and predictive classification.
Bioinform., 2011


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