<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Krause, Rolf</dc:contributor>
  <dc:contributor>Gonzalez, Santiago Fernandez</dc:contributor>
  <dc:creator>Pizzagalli, Diego Ulisse</dc:creator>
  <dc:date>2020-02-19</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The immune system has a critical role in diseases of primary importance such as infections and cancer.  Hence, it represents a target for novel therapeutic strategies. However, the immune system relies on a  complex network of cell-to-cell interactions which remains largely unknown, or difficult to be interpreted. The  combination of experimental data with computational methods is of paramount importance to analyze these  interactions. Indeed, recently established 2-photon intravital microscopes (2P-IVM), can capture videos of  cells while interacting in organs of living animals. These interactions are often associated with specific  movement patterns. Hence, computer vision methods have the potential to extract knowledge from these  videos by analyzing the movement of cells. Unfortunately, common analysis methods poorly apply to 2P-IVM  videos capturing the cells of the immune system. This is mainly due to the complex appearance and  biomechanical properties of these cells, as well as challenges introduced by in vivo imaging. Additionally, a  lack of publicly available 2P-IVM datasets hampers the development of novel analysis methods along with  data-driven studies of the immune system. Finally, common measures of cell motility, poorly describe the  dynamic behavior of immune cells. In this thesis, we address these limitations by • Making available the first  database of 2P-IVM videos and tracks of immune cells. • Modeling as graph the content of 2P-IVM videos,  from pixels to biological processes. • Developing, refining, and applying a variety of computational methods  to extract knowledge from this graph. • Shifting the analysis of cell motility towards the recognition of cell  actions, which does not necessarily require cell tracking. This combination of microscopy data, graph-based  methods, and action-based models allowed us to quantify the complex movement patterns of neutrophils,  revealing different phases of the immune response to influenza vaccination.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1319237</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/319237</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/319237/files/2020INFO018.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:rero-006-118977</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1319237</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Systems biology</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Immunology</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Cell behavior</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Graph-based methods</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Action recognition</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Microscopy</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/004</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">A hierarchy of graph-based methods to study the behavior of immune cells in vivo</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_db06</dc:type>
</oai_dc:dc>
