H. Robert Frost

Orcid: 0000-0002-6794-9945

Affiliations:
  • Dartmouth College, Hanover, NH, USA


According to our database1, H. Robert Frost authored at least 27 papers between 2005 and 2024.

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

Timeline

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Online presence:

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Bibliography

2024
CAraCAl: CAMML with the integration of chromatin accessibility.
BMC Bioinform., December, 2024

A generalized eigenvector centrality for multilayer networks with inter-layer constraints on adjacent node importance.
Appl. Netw. Sci., December, 2024

Tissue-adjusted pathway analysis of cancer (TPAC): A novel approach for quantifying tumor-specific gene set dysregulation relative to normal tissue.
PLoS Comput. Biol., January, 2024

Network analysis using Krylov subspace trajectories.
CoRR, 2024

2023
STREAK: A supervised cell surface receptor abundance estimation strategy for single cell RNA-sequencing data using feature selection and thresholded gene set scoring.
PLoS Comput. Biol., 2023

Eigenvector Centrality for Multilayer Networks with Dependent Node Importance.
Proceedings of the Complex Networks & Their Applications XII, 2023

2022
CAMML with the Integration of Marker Proteins (ChIMP).
Bioinform., November, 2022

Eigenvectors from Eigenvalues Sparse Principal Component Analysis.
J. Comput. Graph. Stat., January, 2022

CBEA: Competitive balances for taxonomic enrichment analysis.
PLoS Comput. Biol., 2022

Iterative execution of discrete and inverse discrete Fourier transforms with applications for signal denoising via sparsification.
CoRR, 2022

2021
Analyzing cancer gene expression data through the lens of normal tissue-specificity.
PLoS Comput. Biol., 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

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

Computation and application of tissue-specific gene set weights.
Bioinform., 2018

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

2015
An Independent Filter for Gene Set Testing Based on Spectral Enrichment.
IEEE ACM Trans. Comput. Biol. Bioinform., 2015

Modeling Neurovascular Coupling from Clustered Parameter Sets for Multimodal EEG-NIRS.
Comput. Math. Methods Medicine, 2015

Spectral gene set enrichment (SGSE).
BMC Bioinform., 2015

Principal component gene set enrichment (PCGSE).
BioData Min., 2015

2014
Modeling the Autism Spectrum Disorder Phenotype.
Neuroinformatics, 2014

Optimization of gene set annotations via entropy minimization over variable clusters (EMVC).
Bioinform., 2014

2012
Markov Chain Ontology Analysis (MCOA).
BMC Bioinform., 2012

Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALS.
BioData Min., 2012

2009
A journey to Semantic Web query federation in the life sciences.
BMC Bioinform., 2009

2005
Application of Information Technology: MediClass: A System for Detecting and Classifying Encounter-based Clinical Events in Any Electronic Medical Record.
J. Am. Medical Informatics Assoc., 2005


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