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In this case, sample size. OK, once we have everything in place, including sample size, we need to expand this out to have some number of samples for each n.

Ok, so I have a MTHFR C677T homozygous mutation

For that, we can use the function in tidyr same library as crossings , expand. Now, if we want to simulate each of these, say, times, we need to assign unique sim numbers, so for each n and sim number we have a unique data set.


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We can use crossing to replicate each combination of variables above some number of times. Use low numbers of simulation for development, then crank them up for final analysis. Great — almost ready to go! Now we just need to add in fitted values.

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Fortunately, as rnorm works with vectors, we can just use a mutate here. First, we now need to generate a lot of fit models. Second, the map function in the purrr library allows us to iterate over different levels or grouped data frames, and perform some function.


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This is a new weird set of functions. What can you query on the same table and what you can not , it's not clear for me. You can't query a table in row level triggers on the same table, except in insert triggers when the insert being run is a single row insert insert values, FOR ALL I think should check I know , it's batched but does one row at a time.

Basically if you're doing a single row insert then oracle knows, without having to check what data is affected, that the table isn't mutating in any meaningful way.

Those that started as programmers myself usually tend to thing in "programming" at the moment of solving any issue, but we have to take into account all the features the DB provides! Function based indexes can help a lot to avoid having to deal with complex triggers, I've found them to be a great tool that you have to consider!

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I'd certainly never code insert triggers that query the table because even if I'm only doing single row inserts right now, at some point in the future I may well want to do a multi-row insert. Error: You don't have JavaScript enabled. There are programs listed below that can help you compare your results to a typical human genome and identify where you differ.

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The differences you find are genetic mutations. Once you have your raw data, upload it here for methylation interpretation:. The gold standard is to work with an experienced MTHFR practitioner to determine an effective course of action for your unique genetic makeup. Making Bulletproof choices in diet, supplementation, and lifestyle provides a kick-ass antidote to the MTHFR mutation! If you have the MTHFR gene defect, please share your experiences to help readers know what has been the most useful information for you.

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