Mikhail G. Dozmorov

Orcid: 0000-0002-0086-8358

Affiliations:
  • Virginia Commonwealth University, Department of Biostatistics, Richmond, VA, USA


According to our database1, Mikhail G. Dozmorov authored at least 28 papers between 2007 and 2024.

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

Timeline

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Bibliography

2024
Machine and deep learning methods for predicting 3D genome organization.
CoRR, 2024

2023
bootRanges: flexible generation of null sets of genomic ranges for hypothesis testing.
Bioinform., May, 2023

matchRanges: generating null hypothesis genomic ranges via covariate-matched sampling.
Bioinform., May, 2023

excluderanges: exclusion sets for T2T-CHM13, GRCm39, and other genome assemblies.
Bioinform., April, 2023

2022
preciseTAD: a transfer learning framework for 3D domain boundary prediction at base-pair resolution.
Bioinform., 2022

2020
A method for estimating coherence of molecular mechanisms in major human disease and traits.
BMC Bioinform., 2020

Correction to: SpectralTAD: an R package for defining a hierarchy of topologically associated domains using spectral clustering.
BMC Bioinform., 2020

SpectralTAD: an R package for defining a hierarchy of topologically associated domains using spectral clustering.
BMC Bioinform., 2020

2019
multiHiCcompare: joint normalization and comparative analysis of complex Hi-C experiments.
Bioinform., 2019

Disease classification: from phenotypic similarity to integrative genomics and beyond.
Briefings Bioinform., 2019

2018
HiCcompare: an R-package for joint normalization and comparison of HI-C datasets.
BMC Bioinform., 2018

2017
Proceedings of the 2017 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2017

Epigenomic annotation-based interpretation of genomic data: from enrichment analysis to machine learning.
Bioinform., 2017

2016
Proceedings of the 2016 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2016

Improving sensitivity of linear regression-based cell type-specific differential expression deconvolution with per-gene vs. global significance threshold.
BMC Bioinform., 2016

GenomeRunner web server: regulatory similarity and differences define the functional impact of SNP sets.
Bioinform., 2016

2015
Detrimental effects of duplicate reads and low complexity regions on RNA- and ChIP-seq data.
BMC Bioinform., December, 2015

2014
Proceedings of the 2014 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2014

2013
Proceedings of the 2013 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2013

mirCoX: a database of miRNA-mRNA expression correlations derived from RNA-seq meta-analysis.
BMC Bioinform., 2013

Systematic classification of non-coding RNAs by epigenomic similarity.
BMC Bioinform., 2013

2012
Proceedings of the 2012 MidSouth computational biology and bioinformatics society (MCBIOS) conference.
BMC Bioinform., 2012

Genome<i>Runner</i>: automating genome exploration.
Bioinform., 2012

2011
Proceedings of the 2011 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2011

High-throughput processing and normalization of one-color microarrays for transcriptional meta-analyses.
BMC Bioinform., 2011

Predicting gene ontology from a global meta-analysis of 1-color microarray experiments.
BMC Bioinform., 2011

2008
From microarray to biology: an integrated experimental, statistical and in silico analysis of how the extracellular matrix modulates the phenotype of cancer cells.
BMC Bioinform., 2008

2007
Systems biology approach for mapping the response of human urothelial cells to infection by <i>Enterococcus faecalis</i>.
BMC Bioinform., 2007


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