Christopher I. Amos

According to our database1, Christopher I. Amos authored at least 22 papers between 1999 and 2022.

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Bibliography

2022
Iam hiQ - a novel pair of accuracy indices for imputed genotypes.
BMC Bioinform., 2022

2021
Lessons Learned from an Enterprise-Wide Clinical Datathon.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021

2020
Cancer prognosis prediction using somatic point mutation and copy number variation data: a comparison of gene-level and pathway-based models.
BMC Bioinform., 2020

Comparison of pathway and gene-level models for cancer prognosis prediction.
BMC Bioinform., 2020

2019
An accurate and powerful method for copy number variation detection.
Bioinform., 2019

2018
Gene characteristics predicting missense, nonsense and frameshift mutations in tumor samples.
BMC Bioinform., 2018

A multi-omics approach for identifying important pathways and genes in human cancer.
BMC Bioinform., 2018

An Efficient Survival Multifactor Dimensionality Reduction Method for Detecting Gene-Gene Interactions of Lung Cancer Onset Age.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2018

2017
Pathway-Based Kernel Boosting for the Analysis of Genome-Wide Association Studies.
Comput. Math. Methods Medicine, 2017

seXY: a tool for sex inference from genotype arrays.
Bioinform., 2017

2016
FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data.
BMC Bioinform., 2016

Unsupervised gene set testing based on random matrix theory.
BMC Bioinform., 2016

Component-wise gradient boosting and false discovery control in survival analysis with high-dimensional covariates.
Bioinform., 2016

2014
Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors.
BioData Min., 2014

2012
Derived SNP Alleles are Used More Frequently than Ancestral Alleles as Risk-associated Variants in Common Human Diseases.
J. Bioinform. Comput. Biol., 2012

2011
Genome-wide algorithm for detecting CNV associations with diseases.
BMC Bioinform., 2011

2010
Forward-time simulation of realistic samples for genome-wide association studies.
BMC Bioinform., 2010

2009
Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide.
Comput. Stat. Data Anal., 2009

2008
Forward-time simulations of non-random mating populations using simuPOP.
Bioinform., 2008

2006
Strategies to Improve Healthcare Websites.
Proceedings of the AMIA 2006, 2006

2005
An Informatics Tool to Assess Individualized Colon Cancer Risk.
Proceedings of the AMIA 2005, 2005

1999
KinSys: A Database Management Application.
Proceedings of the AMIA 1999, 1999


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