Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2023Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning17citations

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Peterson, Bennet
1 / 1 shared
Yandell, Mark
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Kingsmore, Stephen F.
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Brunelli, Luca
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Moore, Barry
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2023

Co-Authors (by relevance)

  • Peterson, Bennet
  • Yandell, Mark
  • Kingsmore, Stephen F.
  • Brunelli, Luca
  • Moore, Barry
  • Jenkins, Sabrina Malone
  • Oriol, Albert
  • Hobbs, Charlotte
  • Hernandez, Edgar Javier
  • Bainbridge, Matthew N.
  • Sanford, Erica
  • Zoucha, Samuel
  • Rosales, Edwin
OrganizationsLocationPeople

article

Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

  • Peterson, Bennet
  • Yandell, Mark
  • Kingsmore, Stephen F.
  • Frise, Erwin
  • Brunelli, Luca
  • Moore, Barry
  • Jenkins, Sabrina Malone
  • Oriol, Albert
  • Hobbs, Charlotte
  • Hernandez, Edgar Javier
  • Bainbridge, Matthew N.
  • Sanford, Erica
  • Zoucha, Samuel
  • Rosales, Edwin
Abstract

<jats:title>Abstract</jats:title><jats:sec><jats:title>Background</jats:title><jats:p>Rapidly and efficiently identifying critically ill infants for whole genome sequencing (WGS) is a costly and challenging task currently performed by scarce, highly trained experts and is a major bottleneck for application of WGS in the NICU. There is a dire need for automated means to prioritize patients for WGS.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Institutional databases of electronic health records (EHRs) are logical starting points for identifying patients with undiagnosed Mendelian diseases. We have developed automated means to prioritize patients for rapid and whole genome sequencing (rWGS and WGS) directly from clinical notes. Our approach combines a clinical natural language processing (CNLP) workflow with a machine learning-based prioritization tool named <jats:italic>Mendelian Phenotype Search Engine</jats:italic> (MPSE).</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>MPSE accurately and robustly identified NICU patients selected for WGS by clinical experts from Rady Children’s Hospital in San Diego (AUC 0.86) and the University of Utah (AUC 0.85). In addition to effectively identifying patients for WGS, MPSE scores also strongly prioritize diagnostic cases over non-diagnostic cases, with projected diagnostic yields exceeding 50% throughout the first and second quartiles of score-ranked patients.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>Our results indicate that an automated pipeline for selecting acutely ill infants in neonatal intensive care units (NICU) for WGS can meet or exceed diagnostic yields obtained through current selection procedures, which require time-consuming manual review of clinical notes and histories by specialized personnel.</jats:p></jats:sec>

Topics
  • impedance spectroscopy
  • size-exclusion chromatography
  • machine learning