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Manolis Kellis

Researcher at Massachusetts Institute of Technology

Publications -  448
Citations -  132627

Manolis Kellis is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Gene & Genome. The author has an hindex of 128, co-authored 405 publications receiving 112181 citations. Previous affiliations of Manolis Kellis include Broad Institute & Epigenomics AG.

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Pan-cancer screen for mutations in non-coding elements with conservation and cancer specificity reveals correlations with expression and survival.

TL;DR: The screen for significant mutation patterns coupled with correlative mutational analysis identified new individual driver candidates and suggest that some non-coding mutations recurrently affect expression and play a role in cancer development.
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The evolutionary dynamics of the Saccharomyces cerevisiae protein interaction network after duplication

TL;DR: It is found that the predicted frequency of self-interactions in the preduplication network is significantly higher than that observed in today's network, which could suggest a structural difference between the modern and ancestral networks, preferential addition or retention of interactions between ohnologs, or selective pressure to preserve duplicates ofSelf-interacting proteins.
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Systematic chromatin state comparison of epigenomes associated with diverse properties including sex and tissue type

TL;DR: ChromDiff is presented, a group-wise chromatin state comparison method that generates an information-theoretic representation of epigenomes and corrects for external covariate factors to better isolate relevant Chromatin state changes.
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Most parsimonious reconciliation in the presence of gene duplication, loss, and deep coalescence using labeled coalescent trees

TL;DR: This work presents a novel algorithm, DLCpar, that achieves high accuracy, comparable to sophisticated probabilistic reconciliation methods, at reduced run time and with far fewer parameters, which enable inferences of the complex evolution of gene families across a broad range of species and large data sets.