phyloseq | analyze phylogenetic sequencing data ; and to reproducibly | Genomics library
kandi X-RAY | phyloseq Summary
kandi X-RAY | phyloseq Summary
McMurdie and Holmes (2014) Shiny-phyloseq: Web Application for Interactive Microbiome Analysis with Provenance Tracking. Bioinformatics (Oxford, England) 31(2), 282–283. McMurdie and Holmes (2013) phyloseq: An R package for reproducible interactive analysis and graphics of microbiome census data PLoS ONE 8(4):e61217.
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Community Discussions
Trending Discussions on phyloseq
QUESTION
Here is a working example of what I want to do.
...ANSWER
Answered 2021-Jun-02 at 07:37A solution offered by the authors of the phyloseq package:
QUESTION
I tried to extract the nrow inside of a loop but it keep the same number of the last count for all interactions of the loop, the problem correspond to the lines
...ANSWER
Answered 2021-Apr-20 at 23:24The fix based on the code showed will be the same as the one used for initialization of 'group1', 'group2' etc. i.e. create an empty vector for 'n1', 'n2' and rbind
or c
QUESTION
I need to convert my OTU table from my phyloseq object into a data frame so that I can use it to run PICRUSt2, but as.data.frame(physeq@otu_table)
won't make it a data frame. I tried pie<-as.matrix(physeq@otu_table)
and when I say is.matrix(pie) #it says TRUE
, but when I say class(pie) #it says [1] "otu_table" attr(,"package") [1] "phyloseq"
It wont even pretend to be a data frame:
ANSWER
Answered 2021-Mar-09 at 08:33Sorry I don't have enough information to properly help you, but have you ever tried to use as_tibble() from the tidyverse package, instead of as_dataframe() ?
QUESTION
I am trying to change text label sizes inside my plot (not the axes, rather the label annotations)
I am working with a phyloseq object but I don't think that matters. Here is the code and the output. Any suggestions?
...ANSWER
Answered 2020-Aug-27 at 12:53Looks like size for the text label is a fixed value 2, in the plot_ordination() function see L1135 at GitHub in plot-methods.R file
QUESTION
I analyse microbiome data using
...ANSWER
Answered 2020-Aug-24 at 09:24Yes, as illustrated in the vignette http://bioconductor.org/packages/release/bioc/vignettes/DirichletMultinomial/inst/doc/DirichletMultinomial.pdf section 2 and in your code it is possible to run on multiple cores.
Probably what is happening is that there are errors for some of the values of X; what is the value of fit? Also, one might try
QUESTION
I am using plot_bar function in R to illustrate some data from a phyloseq class. I want to add some different colors to my plot, here the pallette Paired from the RColorBrewer package. For some reasons the bars end up still having the default color around them. Here you can see how it looks like: https://imgur.com/a/VSBvwtk Any way I could get rid of them?
...ANSWER
Answered 2020-Jul-28 at 12:31You defined color = phylum
in the creation of your plot, but never manually defined the color, so the default is still used. fill
fills the bars with color in a bar plot and color
outlines the bars.
Try adding scale_color_manual(values = NA)
to your plot. Alternatively if you want the outline to match you could use scale_color_brewer(palette = "Paired")
QUESTION
I am trying to write output from permutation analysis by using below code but it shows error, could you please suggest how I can resolve this error?
...ANSWER
Answered 2020-Jul-11 at 22:07The output is not in data.frame format, an option is to capture the output with capture.output
QUESTION
When install any new package I get errors saying Rtools is not found. I followed the manual install instructions for Rtools but still get the same error message.
...ANSWER
Answered 2020-Jun-19 at 12:14After installation is complete, you need to perform one more step to be able to compile R packages: you need to put the location of the Rtools make utilities (bash, make, etc) on the PATH. The easiest way to do so is create a text file .Renviron in your Documents folder which contains the following line:
QUESTION
I am currently trying to knit an R markdown document to html (or pdf) where in a certain chunk I generate multiple plots. I specify the captions through the fig.cap
argument in the chunk options with a vector of the same length as the number of plots. However, for this to work the chunk option message
has to be TRUE
.
The issue starts when a ggplot2 object is generated by a function in the chunk and I want to apply a new fill with viridis::scale_fill_viridis
. Which is fine, but inevitably throws a message/warning that there is already a fill applied to the ggplot2 object and that the viridis will replace it (Scale for 'fill' is already present. Adding another scale for 'fill', which will replace the existing scale
). I do not want to get this into the output of my markdown html. Using suppressMessages
apparently also suppresses the html (and pdf!) captions.
So my question is: is there a way to "unset" the existing scales attribute to avoid this message being generated? Short from that my only other option would be to dive into the code that generated the object in the first place. Or: is there a way that knitr preserves captions when the chunk option messages=F
?
A minimal working example would be the following code in an R markdown document:
...ANSWER
Answered 2017-Sep-01 at 15:07Take a look at a ggplot object, here p
:
str(p)
There's a lot of sub-structure. Take a look at p$scales
. It's a ScalesList. The following might help you:
i <- which(sapply(p$scales$scales, function(x) 'fill' %in% x$aesthetics))
p$scales$scales[[i]] <- NULL
QUESTION
library(tidyverse)
library(ape)
library(phyloseq)
unifrac_unweighted <- UniFrac(tree, weighted = F)
Fehler in (function (classes, fdef, mtable) : unable to find an inherited method for function ‘UniFrac’ for signature ‘"phylo"’
3.
stop(gettextf("unable to find an inherited method for function %s for signature %s", sQuote(fdef@generic), sQuote(cnames)), domain = NA)
2.
(function (classes, fdef, mtable) { methods <- .findInheritedMethods(classes, fdef, mtable) if (length(methods) == 1L) ...
1.
UniFrac(tree_BLS, weighted = T)
...ANSWER
Answered 2020-Apr-10 at 13:47The UniFrac
function requirs a phyloseq
object:
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