Michael Fernandez

Dr. Michael Fernandez


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
25 August 2014 in The Journal of Physical Chemistry Letters
Verified
Journal Article
Closed access
MFMichael Fernandez
Michael Fernandez
PBPeter G. Boyd
Peter G. Boyd
TDThomas D. Daff
Thomas D. Daff
MAMohammad Zein Aghaji
Mohammad Zein Aghaji
TWTom K. Woo
Tom K. Woo

23 March 2022 in Nature Machine Intelligence
Verified
Journal Article
Closed access
PDF file
MPMohit Pandey
Mohit Pandey
MFMichael Fernandez
Michael Fernandez
FGFrancesco Gentile
Francesco Gentile
OIOlexandr Isayev
Olexandr Isayev
ATAlexander Tropsha
Alexander Tropsha
ACArtem Cherkasov
Artem Cherkasov

4 April 2013 in The Journal of Physical Chemistry C
Verified
Journal Article
Closed access
MFMichael Fernandez
Michael Fernandez
TWTom K. Woo
Tom K. Woo
CWChristopher Wilmer
Christopher Wilmer
RSRandall Snurr
Randall Snurr

17 June 2013 in The Journal of Physical Chemistry C
Verified
Journal Article
Closed access
MFMichael Fernandez
Michael Fernandez
NTNicholas R. Trefiak
Nicholas R. Trefiak
TWTom K. Woo
Tom K. Woo

31 July 2018 in Journal of Chemical Information and Modeling
Verified
Journal Article
Closed access
MFMichael Fernandez
Michael Fernandez
FBFuqiang Ban
Fuqiang Ban
GWGodwin Woo
Godwin Woo
MHMichael Hsing
Michael Hsing
TYTakeshi Yamazaki
Takeshi Yamazaki
ACArtem Cherkasov
Artem Cherkasov

10 February 2012 in Nucleic Acids Research
Verified
Journal Article
Open access
PDF file
MFMichael Fernandez
Michael Fernandez
DMDiego Miranda-Saavedra
Diego Miranda-Saavedra
The chemical modification of histones at specific DNA regulatory elements is linked to the activation, inactivation and poising of genes. A number of tools exist to predict enhancers from chromatin modification maps, but their practical application is limited because they either (i) consider a smaller number of marks than those necessary to define the various enhancer classes or (ii) work with an excessive number of marks, which is experimentally unviable. We have developed a method for chromatin state detection using support vector machines in combination with genetic algorithm optimization, called ChromaGenSVM. ChromaGenSVM selects optimum combinations of specific histone epigenetic marks to predict enhancers. In an independent test, ChromaGenSVM recovered 88% of the experimentally supported enhancers in the pilot ENCODE region of interferon gamma-treated HeLa cells. Furthermore, ChromaGenSVM successfully combined the profiles of only five distinct methylation and acetylation marks from ChIP-seq libraries done in human CD4 + T cells to predict ∼21 000 experimentally supported enhancers within 1.0 kb regions and with a precision of ∼90%, thereby improving previous predictions on the same dataset by 21%. The combined results indicate that ChromaGenSVM comfortably outperforms previously published methods and that enhancers are best predicted by specific combinations of histone methylation and acetylation marks.