phyloseq | analyze phylogenetic sequencing data ; and to reproducibly | Genomics library

 by   joey711 R Version: Current License: No License

kandi X-RAY | phyloseq Summary

kandi X-RAY | phyloseq Summary

phyloseq is a R library typically used in Artificial Intelligence, Genomics applications. phyloseq has no bugs, it has no vulnerabilities and it has low support. You can download it from GitHub.

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.
Support
    Quality
      Security
        License
          Reuse

            kandi-support Support

              phyloseq has a low active ecosystem.
              It has 496 star(s) with 180 fork(s). There are 55 watchers for this library.
              OutlinedDot
              It had no major release in the last 6 months.
              There are 646 open issues and 909 have been closed. On average issues are closed in 84 days. There are 24 open pull requests and 0 closed requests.
              It has a neutral sentiment in the developer community.
              The latest version of phyloseq is current.

            kandi-Quality Quality

              phyloseq has no bugs reported.

            kandi-Security Security

              phyloseq has no vulnerabilities reported, and its dependent libraries have no vulnerabilities reported.

            kandi-License License

              phyloseq does not have a standard license declared.
              Check the repository for any license declaration and review the terms closely.
              OutlinedDot
              Without a license, all rights are reserved, and you cannot use the library in your applications.

            kandi-Reuse Reuse

              phyloseq releases are not available. You will need to build from source code and install.
              Installation instructions, examples and code snippets are available.

            Top functions reviewed by kandi - BETA

            kandi's functional review helps you automatically verify the functionalities of the libraries and avoid rework.
            Currently covering the most popular Java, JavaScript and Python libraries. See a Sample of phyloseq
            Get all kandi verified functions for this library.

            phyloseq Key Features

            No Key Features are available at this moment for phyloseq.

            phyloseq Examples and Code Snippets

            No Code Snippets are available at this moment for phyloseq.

            Community Discussions

            QUESTION

            Non standard evaluation does not work: Error in h(simpleError(msg, call))
            Asked 2021-Jun-02 at 07:38

            Here is a working example of what I want to do.

            ...

            ANSWER

            Answered 2021-Jun-02 at 07:37

            A solution offered by the authors of the phyloseq package:

            Source https://stackoverflow.com/questions/67705772

            QUESTION

            R problems with a count nrow inside of a for loop
            Asked 2021-Apr-20 at 23:24

            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 23:24

            The 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

            Source https://stackoverflow.com/questions/67187342

            QUESTION

            OTU table from phyloseq object can't be coerced into a data frame
            Asked 2021-Mar-09 at 17:06

            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 08:33

            Sorry 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() ?

            Source https://stackoverflow.com/questions/66541417

            QUESTION

            Change size of label annotations in a ggplot
            Asked 2020-Aug-27 at 12:53

            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 12:53

            Looks 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

            Source https://stackoverflow.com/questions/63616148

            QUESTION

            Can `dmn {DirichletMultinomial}` be run on multiple cpu cores in R?
            Asked 2020-Aug-24 at 09:24

            I analyse microbiome data using

            ...

            ANSWER

            Answered 2020-Aug-24 at 09:24

            Yes, 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

            Source https://stackoverflow.com/questions/63557763

            QUESTION

            Removing the original color outline in R when using a new pallette in a barplot
            Asked 2020-Jul-28 at 12:31

            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 12:31

            You 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")

            Source https://stackoverflow.com/questions/63133884

            QUESTION

            error while writing file after adonis analysis
            Asked 2020-Jul-11 at 22:07

            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 22:07

            The output is not in data.frame format, an option is to capture the output with capture.output

            Source https://stackoverflow.com/questions/62854770

            QUESTION

            Rtools not found by R when installing packages from CRAN
            Asked 2020-Jun-19 at 14:12

            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 12:14

            After 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:

            Source https://stackoverflow.com/questions/62469777

            QUESTION

            Unset existing scale_fill_discrete in ggplot2 or suppress message for new scale
            Asked 2020-May-12 at 10:43

            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 15:07

            Take 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

            Source https://stackoverflow.com/questions/45998396

            QUESTION

            unable to find an inherited method for function ‘UniFrac’ for signature ‘"phylo"’
            Asked 2020-Apr-10 at 13:47
            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 13:47

            The UniFrac function requirs a phyloseq object:

            Source https://stackoverflow.com/questions/61140561

            Community Discussions, Code Snippets contain sources that include Stack Exchange Network

            Vulnerabilities

            No vulnerabilities reported

            Install phyloseq

            See the phyloseq installation page for further details, examples.

            Support

            For any new features, suggestions and bugs create an issue on GitHub. If you have any questions check and ask questions on community page Stack Overflow .
            Find more information at:

            Find, review, and download reusable Libraries, Code Snippets, Cloud APIs from over 650 million Knowledge Items

            Find more libraries
            CLONE
          • HTTPS

            https://github.com/joey711/phyloseq.git

          • CLI

            gh repo clone joey711/phyloseq

          • sshUrl

            git@github.com:joey711/phyloseq.git

          • Stay Updated

            Subscribe to our newsletter for trending solutions and developer bootcamps

            Agree to Sign up and Terms & Conditions

            Share this Page

            share link