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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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Relating Whole-Genome Expression Data with Protein-Protein Interactions

TL;DR: The relationship of protein-protein interactions with mRNA expression levels, by integrating a variety of data sources for yeast, is investigated, finding that permanent complexes, such as the ribosome and proteasome, have a particularly strong relationship with expression, while transient ones do not.
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Statistical analysis of amino acid patterns in transmembrane helices: the GxxxG motif occurs frequently and in association with β-branched residues at neighboring positions

TL;DR: The special role for the beta-branched residues Ile and Val suggested here is consistent with the hypothesis that residues with constrained rotameric freedom in helical conformation might reduce the entropic cost of folding in transmembrane proteins.
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PeakSeq enables systematic scoring of ChIP-seq experiments relative to controls.

TL;DR: A general scoring approach to address unique challenges in ChIP-seq data analysis is described, based on the observation that sites of potential binding are strongly correlated with signal peaks in the control, likely revealing features of open chromatin.
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Multi-platform discovery of haplotype-resolved structural variation in human genomes

Mark Chaisson, +107 more
TL;DR: A suite of long-read, short- read, strand-specific sequencing technologies, optical mapping, and variant discovery algorithms are applied to comprehensively analyze three trios to define the full spectrum of human genetic variation in a haplotype-resolved manner.
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Variation in Transcription Factor Binding Among Humans

TL;DR: In this paper, the binding sites of RNA polymerase II (PolII) and a key regulator of immune responses, nuclear factor κB (p65), were mapped in 10 lymphoblastoid cell lines, and 25 and 7.5% of the respective binding regions were found to differ between individuals.