Manolis Kellis

Affiliations:
  • Massachusetts Institute of Technology, Cambridge, USA


According to our database1, Manolis Kellis authored at least 45 papers between 2004 and 2024.

Collaborative distances:

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2024
TrustLLM: Trustworthiness in Large Language Models.
CoRR, 2024

2023
GENCODE: reference annotation for the human and mouse genomes in 2023.
Nucleic Acids Res., January, 2023

Contextualized Machine Learning.
CoRR, 2023

LLMs Understand Glass-Box Models, Discover Surprises, and Suggest Repairs.
CoRR, 2023

Combinatorial Optimization for Predicting Optimal Cell-state Conversion Paths.
Proceedings of the 16th International Congress on Image and Signal Processing, 2023

2021
GENCODE 2021.
Nucleic Acids Res., 2021

NOTMAD: Estimating Bayesian Networks with Sample-Specific Structures and Parameters.
CoRR, 2021

2020
Spectral Alignment of Graphs.
IEEE Trans. Netw. Sci. Eng., 2020

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.
, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
Nat., 2020

2019
Network Infusion to Infer Information Sources in Networks.
IEEE Trans. Netw. Sci. Eng., 2019

GENCODE reference annotation for the human and mouse genomes.
Nucleic Acids Res., 2019

Causal Mediation Analysis Leveraging Multiple Types of Summary Statistics Data.
CoRR, 2019

ncdDetect2: improved models of the site-specific mutation rate in cancer and driver detection with robust significance evaluation.
Bioinform., 2019

2018
Genie: A Secure, Transparent Sharing and Services Platform for Genetic and Health Data.
CoRR, 2018

A latent topic model for mining heterogenous non-randomly missing electronic health records data.
CoRR, 2018

RANGER-DTL 2.0: rigorous reconstruction of gene-family evolution by duplication, transfer and loss.
Bioinform., 2018

2017
Network Maximal Correlation.
IEEE Trans. Netw. Sci. Eng., 2017

2016
HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease.
Nucleic Acids Res., 2016

Spectral Alignment of Networks.
CoRR, 2016

SwiSpot: modeling riboswitches by spotting out switching sequences.
Bioinform., 2016

2015
Integrative analysis of 111 reference human epigenomes Open.
, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
Nat., 2015

Preface: RECOMB/ISCB Systems Biology, Regulatory Genomics, and DREAM 2014 Special Issue.
J. Comput. Biol., 2015

A Perspective on Future Research Directions in Information Theory.
CoRR, 2015

Improved gene tree error correction in the presence of horizontal gene transfer.
Bioinform., 2015

2014
Comparative analysis of metazoan chromatin organization Open.
Nat., 2014

Comparative analysis of regulatory information and circuits across distant species Open.
Nat., 2014

RECOMB/ISCB Systems Biology, Regulatory Genomics, and DREAM 2013 Special Issue.
J. Comput. Biol., 2014

Diversifying Sparsity Using Variational Determinantal Point Processes.
CoRR, 2014

Pareto-optimal phylogenetic tree reconciliation.
Bioinform., 2014

2013
RFECS: A Random-Forest Based Algorithm for Enhancer Identification from Chromatin State.
PLoS Comput. Biol., 2013

Preface: RECOMB Systems Biology, Regulatory Genomics, and DREAM 2012 Special Issue.
J. Comput. Biol., 2013

Reconciliation Revisited: Handling Multiple Optima when Reconciling with Duplication, Transfer, and Loss.
J. Comput. Biol., 2013

Session Introduction.
Proceedings of the Biocomputing 2013: Proceedings of the Pacific Symposium, 2013

2012
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants.
Nucleic Acids Res., 2012

Preface: RECOMB Systems Biology, Regulatory Genomics, and DREAM 2011 Special Issue.
J. Comput. Biol., 2012

Efficient algorithms for the reconciliation problem with gene duplication, horizontal transfer and loss.
Bioinform., 2012

2011
Preface.
J. Comput. Biol., 2011

SubMAP: Aligning Metabolic Pathways with Subnetwork Mappings.
J. Comput. Biol., 2011

PhyloCSF: a comparative genomics method to distinguish protein coding and non-coding regions.
Bioinform., 2011

Discovery and Characterization of Chromatin States for Systematic Annotation of the Human Genome.
Proceedings of the Research in Computational Molecular Biology, 2011

2010
Motif discovery in physiological datasets: A methodology for inferring predictive elements.
ACM Trans. Knowl. Discov. Data, 2010

Information-Theoretic Inference of Gene Networks Using Backward Elimination.
Proceedings of the International Conference on Bioinformatics & Computational Biology, 2010

2008
Performance and Scalability of Discriminative Metrics for Comparative Gene Identification in 12 <i>Drosophila</i> Genomes.
PLoS Comput. Biol., 2008

2007
Network Motif Discovery Using Subgraph Enumeration and Symmetry-Breaking.
Proceedings of the Research in Computational Molecular Biology, 2007

2004
Methods in Comparative Genomics: Genome Correspondence, Gene Identification and Regulatory Motif Discovery.
J. Comput. Biol., 2004


  Loading...