Eric W. Klee

According to our database1, Eric W. Klee authored at least 19 papers between 2005 and 2024.

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Bibliography

2024
A supervised learning method for classifying methylation disorders.
BMC Bioinform., December, 2024

2023
Deep Phenotyping of Non-Alcoholic Fatty Liver Disease Patients with Genetic Factors for Insights into the Complex Disease.
CoRR, 2023

Enhancing Patient Care in Rare Genetic Diseases: An HPO-based Phenotyping Pipeline.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2023

2021
Universally Rank Consistent Ordinal Regression in Neural Networks.
CoRR, 2021

HELLO: improved neural network architectures and methodologies for small variant calling.
BMC Bioinform., 2021

2020
LeafCutterMD: an algorithm for outlier splicing detection in rare diseases.
Bioinform., 2020

2019
Correction to: Recommendations for performance optimizations when using GATK3.8 and GATK4.
BMC Bioinform., 2019

Recommendations for performance optimizations when using GATK3.8 and GATK4.
BMC Bioinform., 2019

A recurrent Markov state-space generative model for sequences.
Proceedings of the 22nd International Conference on Artificial Intelligence and Statistics, 2019

2018
Improving Single-Nucleotide Polymorphism-Based Fetal Fraction Estimation of Maternal Plasma Circulating Cell-Free DNA Using Bayesian Hierarchical Models.
J. Comput. Biol., 2018

Comparative analysis of de novo assemblers for variation discovery in personal genomes.
Briefings Bioinform., 2018

Deep Learning for Better Variant Calling for Cancer Diagnosis and Treatment.
Proceedings of the 23rd Asia and South Pacific Design Automation Conference, 2018

2016
Proceedings of the 15th Annual UT-KBRIN Bioinformatics Summit 2016: Cadiz, KY, USA. 8-10 April 2016.
BMC Bioinform., August, 2016

2014
The Zebrafish GenomeWiki: a crowdsourcing approach to connect the long tail for zebrafish gene annotation.
Database J. Biol. Databases Curation, 2014

2012
SAAP-RRBS: streamlined analysis and annotation pipeline for reduced representation bisulfite sequencing.
Bioinform., 2012

TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data.
Bioinform., 2012

2007
Quantitating tissue specificity of human genes to facilitate biomarker discovery.
Bioinform., 2007

2005
AMOD: a morpholino oligonucleotide selection tool.
Nucleic Acids Res., 2005

Evaluating eukaryotic secreted protein prediction.
BMC Bioinform., 2005


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