1999
DOI: 10.1002/(sici)1097-0320(19990301)35:3<214::aid-cyto4>3.0.co;2-d
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Signal to noise analysis of multiple color fluorescence imaging microscopy

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Cited by 59 publications
(91 citation statements)
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References 14 publications
(9 reference statements)
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“…This classification procedure is the basis for Spectral Karyotyping and for definitive chromosome recognition. 15 The DAPI counterstained image of the same metaphase can be band-enhanced and displayed side by side with the spectral image which greatly facilitates the integration of chromosome band information within the analysis.…”
Section: Spectral Karyotyping (Sky™)mentioning
confidence: 99%
“…This classification procedure is the basis for Spectral Karyotyping and for definitive chromosome recognition. 15 The DAPI counterstained image of the same metaphase can be band-enhanced and displayed side by side with the spectral image which greatly facilitates the integration of chromosome band information within the analysis.…”
Section: Spectral Karyotyping (Sky™)mentioning
confidence: 99%
“…The intensity information was converted into a classification of cells as target or nontarget cells using two commonly used methods: using a fixed threshold above the background level (26) and using a fixed signal-to-noise ratio (14,23,25). To set thresholds, five FISH images from each sample were analyzed manually, and the percentage of target cells based on the number of total cells was calculated for each image.…”
Section: Resultsmentioning
confidence: 99%
“…As noted above, fluorescence intensity varies between experiments, so the threshold is often set manually for each experiment. Another common approach is to set a fixed signal-to-noise ratio (14,23,25). Pernthaler et al used a fixed signal-to-noise ratio and defined the threshold as the mean background gray value of a FISH gray image multiplied by a signal-to-noise factor (25).…”
mentioning
confidence: 99%
“…They depend on the specific spectra that have to be separated and in the case of fluorescence, the complexity is even higher. The fluorochromes have to be excited at certain spectral ranges, which limits the spectral ranges that are available to detection (24). Zimmermann et al (18) have formulated the problem for the case of live-cell spectral imaging which introduces even stronger restrictions on the acquisition times.…”
Section: Spectral Imaging Challenge: Informationmentioning
confidence: 99%