Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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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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Materials Map under construction

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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693.932 PEOPLE
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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2022Exploring domain continuity across BaTiO 3 grain boundaries: theory meets experiment9citations
  • 2022Exploring domain continuity across BaTiO3 grain boundaries: Theory meets experiment9citations
  • 2020Large scale sequencing of SARS-CoV-2 genomes from one region allows detailed epidemiology and enables local outbreak management18citations
  • 2017Polymers of norbornenyl‐4‐phenol: Dissolution rate characteristics, positive tone photo‐patterning, and polymer properties4citations
  • 2015A Microstructural Study on the Observed Differences in Charpy Impact Behavior Between Hot Isostatically Pressed and Forged 304L and 316L Austenitic Stainless Steel33citations
  • 2011Brittle creep in basalt: implications for time-dependent volcano deformationcitations
  • 20084.4,5,5-tetraphenyl-1,3,2-dioxaborolane23citations

Places of action

Chart of shared publication
Holsgrove, Kristina
2 / 3 shared
Arredondo, Miryam
2 / 9 shared
Oreilly, Tamsin
2 / 2 shared
Huber, John
2 / 2 shared
Gholinia, Ali
2 / 39 shared
Woodruff, Danielle
2 / 2 shared
Kandanarachchi, Pramod
1 / 1 shared
Thoresen, Jennifer
1 / 1 shared
Onishi, Osamu
1 / 1 shared
Ikeda, Haruo
1 / 1 shared
Benedikt, George M.
1 / 1 shared
Koronich, Elaine
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Evans, Paul J.
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Brick, Chad M.
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Cooper, Adam J.
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Sherry, Andrew H.
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Cooper, Norman I.
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Dhers, Jean
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Vinciguerra, Sergio
1 / 2 shared
Meredith, Philip
1 / 6 shared
Heap, Michael
1 / 6 shared
Baud, Patrick
1 / 8 shared
Main, Ian
1 / 1 shared
Wernitz, Sm
1 / 1 shared
Fritschi, Cb
1 / 1 shared
Shaver, Michael P.
1 / 28 shared
Westcott, Sa
1 / 1 shared
Decken, A.
1 / 1 shared
Vogels, Cm
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Chart of publication period
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2020
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Co-Authors (by relevance)

  • Holsgrove, Kristina
  • Arredondo, Miryam
  • Oreilly, Tamsin
  • Huber, John
  • Gholinia, Ali
  • Woodruff, Danielle
  • Kandanarachchi, Pramod
  • Thoresen, Jennifer
  • Onishi, Osamu
  • Ikeda, Haruo
  • Benedikt, George M.
  • Koronich, Elaine
  • Evans, Paul J.
  • Brick, Chad M.
  • Cooper, Adam J.
  • Sherry, Andrew H.
  • Cooper, Norman I.
  • Dhers, Jean
  • Vinciguerra, Sergio
  • Meredith, Philip
  • Heap, Michael
  • Baud, Patrick
  • Main, Ian
  • Wernitz, Sm
  • Fritschi, Cb
  • Shaver, Michael P.
  • Westcott, Sa
  • Decken, A.
  • Vogels, Cm
OrganizationsLocationPeople

article

Large scale sequencing of SARS-CoV-2 genomes from one region allows detailed epidemiology and enables local outbreak management

  • Bell, Andrew
Abstract

<jats:p>The COVID-19 pandemic has spread rapidly throughout the world. In the UK, the initial peak was in April 2020; in the county of Norfolk (UK) and surrounding areas, which has a stable, low-density population, over 3,200 cases were reported between March and August 2020. As part of the activities of the national COVID-19 Genomics Consortium (COG-UK) we undertook whole genome sequencing of the SARS-CoV-2 genomes present in positive clinical samples from the Norfolk region. These samples were collected by four major hospitals, multiple minor hospitals, care facilities and community organisations within Norfolk and surrounding areas. We combined clinical metadata with the sequencing data from regional SARS-CoV-2 genomes to understand the origins, genetic variation, transmission and expansion (spread) of the virus within the region and provide context nationally. Data were fed back into the national effort for pandemic management, whilst simultaneously being used to assist local outbreak analyses. Overall, 1,565 positive samples (172 per 100,000 population) from 1,376 cases were evaluated; for 140 cases between two and six samples were available providing longitudinal data. This represented 42.6% of all positive samples identified by hospital testing in the region and encompassed those with clinical need, and health and care workers and their families. 1,035 cases had genome sequences of sufficient quality to provide phylogenetic lineages. These genomes belonged to 26 distinct global lineages, indicating that there were multiple separate introductions into the region. Furthermore, 100 genetically-distinct UK lineages were detected demonstrating local evolution, at a rate of ~2 SNPs per month, and multiple co-occurring lineages as the pandemic progressed. Our analysis: identified a sublineage associated with 6 care facilities; found no evidence of reinfection in longitudinal samples; ruled out a nosocomial outbreak; identified 16 lineages in key workers which were not in patients indicating infection control measures were effective; found the D614G spike protein mutation which is linked to increased transmissibility dominates the samples and rapidly confirmed relatedness of cases in an outbreak at a food processing facility.The large-scale genome sequencing of SARS-CoV-2-positive samples has provided valuable additional data for public health epidemiology in the Norfolk region, and will continue to help identify and untangle hidden transmission chains as the pandemic evolves.</jats:p>

Topics
  • density
  • impedance spectroscopy