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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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 (2/2 displayed)

  • 2023Evaluating the clinical validity of genes related to hemostasis and thrombosis using the ClinGen gene curation framework5citations
  • 2021Abstract 449: A standard operating procedure for the curation of gene fusionscitations

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Schulze, Harald
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Morange, Pierre
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Co-Authors (by relevance)

  • Schulze, Harald
  • Morange, Pierre
  • Megy, Karyn
  • Ross, Justyne E.
  • Mohan, Shruthi
  • Zhang, Jing
  • Morgan, Neil
  • Sullivan, Mia J.
  • Bury, Loredana
  • Lee, Alfred
  • Keenan, Catriona
  • Futchi, Isabella
  • Frantz, Annabelle
  • Gresele, Paolo
  • Mcdougal, Dara
  • Downes, Kate
  • Botero, Juliana Perez
  • Lambert, Michele P.
  • Cooper, Nichola
  • Freson, Kathleen
  • Cattaneo, Marco
  • Zimowski, Karen
OrganizationsLocationPeople

document

Abstract 449: A standard operating procedure for the curation of gene fusions

  • Lin, Wan-Hsin
  • Lee, Jennifer
  • Pallavajjala, Aparna
  • Danos, Arpad
  • Li, Marilyn
  • Coard, Thomas
  • Ritter, Deborah I.
  • Raca, Gordana
  • Sonkin, Dmitriy
  • Xu, Xinjie
  • Kesserwan, Chimene
  • Griffith, Obi
  • Tanska, Anna
  • Ceccarelli, Michele
  • Stenzinger, Albrecht
  • Lu, Anna
  • Rapisardo, Sarah
  • Williams, Heather E.
  • Wagner, Alex H.
  • Baudis, Michael
  • Zhang, Liying
  • Liu, Xuelu
  • Toruner, Gokce
  • Park, Nicole
  • Saliba, Jason
  • Satgunaseelan, Laveniya
  • Sboner, Andrea
  • Horak, Peter
  • Liu, Jie
  • Reich, Christian
  • Roy, Angshumoy
  • Vlachos, Ioannis S.
  • Xu, Huiling
  • Lee, Kristy
  • Terraf, Panieh
  • Zou, Ying S.
  • Ryland, Georgina
  • Freimuth, Robert R.
  • Berlin, Aaron M.
  • Baughn, Linda B.
  • Cameron, Daniel
  • Rehder, Catherine
Abstract

<jats:title>Abstract</jats:title><jats:p>Despite the well-established role of recurrent gene fusions as oncogenic drivers, current practices for characterizing and interpreting gene fusion events in clinical testing and in biomedical literature are inconsistent. From the conceptual definition of gene fusions to the salient elements that characterize these alterations, a lack of community-driven standards for the curation of gene fusions has resulted in a disparate landscape of fusion representations and supporting tools. Consequently, the evidence-based clinical evaluation of gene fusions requires extensive expert review for accurate interpretation of observed gene fusions with respect to putative evidence from biomedical literature. Furthermore, the lack of these standards inhibits the interoperability of tools, resources, and pipelines - impeding data sharing and downstream utility.To address these challenges, a cross-consortia initiative between the Variant Interpretation for Cancer Consortium and ClinGen was formed to develop a standard operating procedure (SOP) for the curation of gene fusions. The SOP is under development by an international and diverse set of experts in the representation, detection, and clinical interpretation of gene fusions. Participating stakeholders across academic, government, and industry sectors showcased challenges and solutions, and participated in community surveys and discussions to define and develop the SOP for this diverse class of alterations.An initial result of this effort was the precise molecular definition of genomic events and features constituting gene fusions. We distinguish these from similar but distinct classes of structural alterations through clinically-relevant examples. Next, we discuss our findings on community practices around the description and evaluation of gene fusions. We provide our recommendations for characterization and representation of gene fusions from these practices, and compare these recommendations to existing variant representation standards and formats (e.g. HGVS variant nomenclature). We also discuss the concurrent application of formats for standardized human- and machine-readable representations of gene fusion events.We conclude with discussion of the salient elements to enable rapid, scalable, and consistent evaluation of fusions curated from the biomedical literature. Recommendations are provided for the standardized capture of these elements to enable both intuitive and precise characterization of this diverse class of alterations in clinical reporting and literature. In summary, we provide a clinical-practice driven framework and nomenclature for gene fusions, including recommendations for human readability, computational precision, and data integrity within the SOP. This work is a substantial advancement towards standardized communication, investigation, and sharing of gene fusion data across clinical and research domains and specialties.</jats:p><jats:p>Citation Format: Alex H. Wagner, Ioannis S. Vlachos, Dmitriy Sonkin, Panieh Terraf, Chimene Kesserwan, Andrea Sboner, Thomas Coard, Christian Reich, Deborah I. Ritter, Peter Horak, Ying S. Zou, Anna Tanska, Aaron M. Berlin, Anna Lu, Daniel Cameron, Heather E. Williams, Wan-Hsin Lin, Gokce Toruner, Arpad Danos, Jason Saliba, Huiling Xu, Xinjie Xu, Georgina Ryland, Michele Ceccarelli, Liying Zhang, Sarah Rapisardo, Catherine Rehder, Xuelu Liu, Aparna Pallavajjala, Nicole Park, Laveniya Satgunaseelan, Kristy Lee, Jie Liu, Obi Griffith, Robert R. Freimuth, Albrecht Stenzinger, Linda B. Baughn, Michael Baudis, Jennifer Lee, Marilyn Li, Angshumoy Roy, Gordana Raca. A standard operating procedure for the curation of gene fusions [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 449.</jats:p>

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  • impedance spectroscopy