rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2006-2-6
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pubmed:abstractText |
Confocal laser scanning microscopy (CLSM) is the method of choice to study interfacial biofilms and acquires time-resolved three-dimensional data of the biofilm structure. CLSM can be used in a multi-channel modus where the different channels map individual biofilm components. This communication presents a novel image quantification tool, PHLIP, for the quantitative analysis of large amounts of multichannel CLSM data in an automated way. PHLIP can be freely downloaded from http://phlip.sourceforge.net.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16412253-10547787,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16412253-10899813,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/16412253-15153691,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/16412253-9812281
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
1472-6785
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1
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pubmed:dateRevised |
2010-9-20
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pubmed:meshHeading |
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pubmed:year |
2006
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pubmed:articleTitle |
Analysis of a marine phototrophic biofilm by confocal laser scanning microscopy using the new image quantification software PHLIP.
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pubmed:affiliation |
Institute for Molecular Systems Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland. lukas.mueller@imsb.biol.ethz.ch
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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