How can we use capture-recapture analysis for evaluating our cancer registry data?

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How to define the sink temperature and film coefficient?

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I got 02 moderator values defining Johnson-Neyman significance regions. Is it an error?

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Does Napabucasin soluble in dichloromethane and in ethanol?

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Which cell line should we use to perform biological dosimetry experiments?

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Is CD44 degraded in lysosome together with hyaluronan after CD44 mediated endocytosis of hyaluronic acid?

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Is it possible that Cancer cells could survive in heparinized blood for 48 hours?

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The PC12 cell line characteristics?

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Can the viability assays (ex: MTT/CCK-8) measure cell proliferation? or are they solely viability assays?

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Brian Cox

I think the main problem with capture-recapture methods is meeting the necessary assumption of the heterogeneity of mixing in the population, so that the recapture is independent of the first capture.

Alireza Mosavi Jarrahi

You need to make sure you understand the underlying assumption of capture-recapture. In the R library there are few packages that will help you to do the analysis.