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### Description of the bug
Hi, there. Thank you for bringing us this magic tool to accelerate amplicon sequence analysis! Recently I caught an error when running the module qiime2 diversity core. T…
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I want to be able to override the rarefaction depth selected by nf-core/ampliseq. Sometimes the minimum number of ASV identified (the default) is not the optimum value so I would prefer if the user wa…
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You set 1000 cells as default. I was wondering why , and what would be the range of cells in a normal RnaSeq ?
What would be the equivalent in terms of read count also for 1000 cells ? Have you an id…
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Hello, I am trying to extract the density value from a 2D polar map representing an equatorial cut of MAS data.
I obtained the location of Earth at the same time of the MAS data file and I rotated th…
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Rarefaction being random can misrepresent the diversity of samples, using a method like [SRS](https://github.com/vitorheidrich/SRS) which has a [qiime plugin](https://github.com/vitorheidrich/q2-srs) …
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hello, I get the same error. I check the node number in the tree, the number isn't abnormally low compared to the tip number.
the code like this
----bMPD bin i=15 in 435 ---- Tue Aug 1 21:42:1…
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MIght not have got a long enough debug.
```
some dried plovik
some grain alcohol
some borax flux
some moisturizing ointment
some moisturizing ointment
some itch salve
some dried…
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Hi Russel,
Thank you for the package.
As the title suggested, the R squared value differed from those of other packages, such as iCAMP's snm and reltools' fit_sncm when tested on the same datase…
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Coded up a script to overlap terrestrial area of habitat (AOH) with crop production for salmon feed.
Here is how production of soy protein concentrate (SPC) in our plant dominant diet using mass al…
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it look wrong at line 529 in metontiime2.nf make me cannot run diverrsity step. So, i fixed it and run it is successfull. Please, check it.
this is my error:
Caused by:
Process `diversityAnalyses…