<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-18T19:25:26Z</responseDate><request verb="GetRecord" identifier="oai:digital.lib.washington.edu:1773/52580" metadataPrefix="dim">https://digital.lib.washington.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:digital.lib.washington.edu:1773/52580</identifier><datestamp>2026-02-15T21:17:23Z</datestamp><setSpec>com_1773_4888</setSpec><setSpec>col_1773_4943</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Baker, David</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Humphreys, Ian</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2024-10-16T03:16:56Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2024-10-16T03:16:56Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2024-10-16</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">2024</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="other">Humphreys_washington_0250E_27510.pdf</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1773/52580</dim:field>
   <dim:field mdschema="dc" element="description">Thesis (Ph.D.)--University of Washington, 2024</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">The total set of potential protein-protein interactions (PPI) within an organism's proteome guides a plethora of potential biological processes at an organism’s disposal. Understanding these PPIs is critical to our understanding of biological systems, however identifying interactions with high accuracy is challenging. Medium to high-throughput experimental techniques for identifying protein interactions result in high rates of false-negatives and false-positives. However, protein interactions are typically evolutionarily conserved resulting in co-varying mutations at the interface between complexes. Deep learning based protein structure prediction models capture coevolutionary information at significantly higher resolution than statistical methods and we exploit this coevolutionary signal to computationally predict protein-protein interactions with high accuracy based on gold-standard benchmarks. We create and apply bioinformatic and deep learning pipelines to rapidly predict proteome-wide protein-protein interactions in Bacteria and Eukaryotes to identify novel interactions and provide high resolution structural models to better understand their biological ramifications.</dim:field>
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   <dim:field mdschema="dc" element="language" qualifier="iso">en_US</dim:field>
   <dim:field mdschema="dc" element="rights">CC BY</dim:field>
   <dim:field mdschema="dc" element="subject">Biochemistry</dim:field>
   <dim:field mdschema="dc" element="subject">Bioinformatics</dim:field>
   <dim:field mdschema="dc" element="subject">Microbiology</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other">Molecular and cellular biology</dim:field>
   <dim:field mdschema="dc" element="title">Deep learning and coevolution reveal proteome-wide protein-protein interactions</dim:field>
   <dim:field mdschema="dc" element="type">Thesis</dim:field>
   <dim:field mdschema="dc" element="embargo" qualifier="terms">Open Access</dim:field>
   <dim:field mdschema="others" element="access-status">open.access</dim:field>
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