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Mark Gerstein

Researcher at Yale University

Publications -  802
Citations -  172183

Mark Gerstein is an academic researcher from Yale University. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 168, co-authored 751 publications receiving 149578 citations. Previous affiliations of Mark Gerstein include Rutgers University & Structural Genomics Consortium.

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Keeping the shape but changing the charges: A simulation study of urea and its iso-steric analogs

TL;DR: In this paper, the authors compare two possible potentials for urea; one based directly on a parameterization for proteins and another generated from ab initio, quantum calculations, and find that both potentials reproduce essentially the same observed water structure (as evident in radial distribution functions).
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The current excitement in bioinformatics-analysis of whole-genome expression data: how does it relate to protein structure and function?

TL;DR: Whole-genome expression profiles provide a rich new data-trove for bioinformatics and initial analyses of the profiles have included clustering and cross-referencing to 'external' information on protein structure and function.
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Repeat associated mechanisms of genome evolution and function revealed by the Mus caroli and Mus pahari genomes.

TL;DR: In this article, the authors compared the evolutionary dynamics between the Muridae and Hominidae and found that the divergence times between the two families are similar in divergence times to each other, and that the relative rates of nucleotide change and feature turnover in both neutral and functional sequences of the two groups are similar.
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Machine learning and genome annotation: a match meant to be?

TL;DR: Some key aspects of machine learning that make it useful for genome annotation, with illustrative examples from ENCODE are explained.
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Structural proteomics: prospects for high throughput sample preparation

TL;DR: The major challenge facing biologists in the next decade will be to ‘‘finish the job’’, that is, to ascribe a function to each of the proteins that have been discovered.