Dekonvolution von Mikroskopiedaten bei niedrigem Signal-Rausch-Verhältnis
Dekonvolution von Mikroskopiedaten bei niedrigem Signal-Rausch-Verhältnis
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
German
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Subjects
More information
Scope and Contents
Contents
Fluorescence live cell microscopy is central to the analysis of inter- and intracellular signaling. However, analysis of highly dynamic, local processes requires high temporal and spatial resolution imaging, which is intrinsically linked to a low signal-to-noise ratio. To improve image quality after data acquisition, computational techniques, refer...
Alternative Titles
Full title
Dekonvolution von Mikroskopiedaten bei niedrigem Signal-Rausch-Verhältnis
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_2737285916
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2737285916
Other Identifiers
ISSN
0947-0867
E-ISSN
1868-6249
DOI
10.1007/s12268-022-1850-2
