rna | test runner for modern modules | Runtime Evironment library

 by   chialab JavaScript Version: @chialab/wds-plugin-rna@0.16.1 License: MIT

kandi X-RAY | rna Summary

kandi X-RAY | rna Summary

rna is a JavaScript library typically used in Server, Runtime Evironment, Webpack, Nodejs, Boilerplate, Jest applications. rna has no bugs, it has no vulnerabilities, it has a Permissive License and it has low support. You can install using 'npm i @ankumo/esbuild-plugin-html' or download it from GitHub, npm.

We built RNA to be pluggable and to be interoperable with other build systems. A lot of esbuild and postcss plugins are distribuited as standalone packages in order to be reused outside the RNA opinionated ecosystem. We also designed a micro-sdk for esbuild plugin authors that handles transform pipelines and emits chunks or files.
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            kandi-support Support

              rna has a low active ecosystem.
              It has 138 star(s) with 15 fork(s). There are 2 watchers for this library.
              OutlinedDot
              It had no major release in the last 12 months.
              There are 5 open issues and 49 have been closed. On average issues are closed in 106 days. There are 2 open pull requests and 0 closed requests.
              It has a neutral sentiment in the developer community.
              The latest version of rna is @chialab/wds-plugin-rna@0.16.1

            kandi-Quality Quality

              rna has no bugs reported.

            kandi-Security Security

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

            kandi-License License

              rna is licensed under the MIT License. This license is Permissive.
              Permissive licenses have the least restrictions, and you can use them in most projects.

            kandi-Reuse Reuse

              rna releases are available to install and integrate.
              Deployable package is available in npm.
              Installation instructions are not available. Examples and code snippets are available.

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            rna Key Features

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            rna Examples and Code Snippets

            No Code Snippets are available at this moment for rna.

            Community Discussions

            QUESTION

            snakemake - Missing input files for rule salmon_quant: error
            Asked 2021-Jun-10 at 20:38

            I am trying to process bulk RNA-seq data using salmon through snakemake in the conda/mamba environment.

            I am receiving the following error when running snakemake:

            ...

            ANSWER

            Answered 2021-Jun-10 at 20:38

            I think the Snakefile is ok, SRR3350597_GSM2112330_RA_hip_3_Homo_sapiens_RNA-Seq_1.fastq.gz is simply missing. See the ls output of yours, that file is not in it.

            Source https://stackoverflow.com/questions/67927314

            QUESTION

            can only concatenate str (not "bytes") to str
            Asked 2021-Jun-06 at 12:19

            I am using a cellranger mkref and faced with a strange python problem with GTF (custom gtf file):

            ...

            ANSWER

            Answered 2021-May-26 at 21:50

            Python 3 treats strings of bytes as a different object from strings of characters. The distinction matters, since a given string of characters can be encoded to bytes in different ways. E.g. in UTF-8, ä is the two bytes c3 a4 (in hex), while in ISO-8859-1 (Latin 1), it's just the single byte e4.

            Like the comment from @Theophrastus says, subprocess.check_output() returns bytes, matching the low-level API. You need to decode it to characters based on what the expected encoding is. E.g.

            Source https://stackoverflow.com/questions/67859031

            QUESTION

            Problem with plotting an axis that consists of the number of observations by another column
            Asked 2021-Jun-04 at 06:31

            I have a dataset that shows the human chromosomes with their length (which is here named "value") and their respective genes. Furthermore the genes are divided in 4 groups (gtype) which are RNA, prot-coding, pseudogene and rest. I want to plot the individual chromosomes on the y axis and on the x axis I want to have the density of the chromosomes (which would be "the number of genes per chromosome" divided by the length of the chromosome)with a geom_point,bar or col, then make a facet_wrap based on the gtype of the genes. So 4 plots with one plot only counting RNA genes divided by the value, one plot ony counting the prot-coding genes divided by value.

            The plot just divides the total number of all genes by the individual values (it is however normal that chrM would be the biggest)

            However I constantly fail at the x axis and I don't know how to get a plot that makes sense. What I have tried so far is a mix of sum(), count(), nrow() and group_by(). Often the x axis is just the total numbers of rows divided by the "value" or the results don't make sense.

            ...

            ANSWER

            Answered 2021-Jun-03 at 22:19

            If I understand what you're doing correctly, your data looks a bit like this:

            Source https://stackoverflow.com/questions/67828459

            QUESTION

            cellranger: how to convert a gtf file to string
            Asked 2021-Jun-01 at 20:27

            I am using a cellranger mkref and faced with a strange python problem with GTF (custome gtf):

            ...

            ANSWER

            Answered 2021-Jun-01 at 20:27

            I encountered the same issue. The problem was in duplicated IDs in my GTF file. Removing those duplicates solved the issue. See the discussion on Cellranger GitHub: https://github.com/10XGenomics/cellranger/issues/125

            Source https://stackoverflow.com/questions/67706086

            QUESTION

            How do I make the name of a list the name of its column?
            Asked 2021-May-25 at 16:11

            I have a set of 270 RNA-seq samples, and I have already subsetted out their expected counts using the following code:

            ...

            ANSWER

            Answered 2021-May-12 at 18:35

            If we want to name the list, loop over the list, extract the first element of 'expected_count' ('nm1') and use that to assign the names of the list

            Source https://stackoverflow.com/questions/67508574

            QUESTION

            invalid factor level, NA generated in the table
            Asked 2021-May-24 at 10:06

            I am trying to find names in one column and replace with it another column. Here is an example:

            ...

            ANSWER

            Answered 2021-May-24 at 10:06

            Elya, you can simplify what you want to do. Most importantly, you do not need to loop over your data.
            I assume your example data is representative for your dataset. In particular, the information in other is separated by a semi-colon. In this case you can split the string by it and extract from your 3rd column the part required to add to the "gene_id" fragment in your 2nd column. Based on your comment I append a solution for multiple hits in the other column.

            Note: the following names these columns "info", "gene_id", and "other". Make sure to adapt the variable naming.

            data

            Source https://stackoverflow.com/questions/67557794

            QUESTION

            How to unify the number of non-NA cells in raster stack?
            Asked 2021-May-18 at 23:40

            I have raster files that have the same resolution and extent but differ in the number of NA. I want to unify the number of NA between all of them. Is it possible to do it by considering a cell as non-NA if it's not NA in all the raster files?

            Here an example :

            ...

            ANSWER

            Answered 2021-May-18 at 23:40

            It can be a bit confusing to use raster and terra together, so I will just use terra (but you can do the same with raster, using stack in stead of c and cellStats in stead of global.

            Your example data

            Source https://stackoverflow.com/questions/67592103

            QUESTION

            How to associate two lists or columns?
            Asked 2021-Apr-29 at 16:59

            Code/Program:

            ...

            ANSWER

            Answered 2021-Apr-29 at 16:59

            Your code is somewhat inefficient in the sense that it repeatedly splits the all the lines up. In the code below, this is only done once when they are first read in from the file. In addition, after reading they're transposed into columns of row since most of the processing is done with respect to what in each column.

            Source https://stackoverflow.com/questions/67309853

            QUESTION

            How to get unique values/elements of a column?
            Asked 2021-Apr-27 at 15:49

            I am trying to get the unique values of a column from a tab. The values are repeated and the file has 1,000+ lines, I just want to have the names of the values, not all, and the ones that are repeated. I'm working on my code, but when I do "RUN" it generates the separate and random letters of the values (see example in 'Output' below). I hope someone can help me find my mistake. Please and thank you very much!

            Code:

            ...

            ANSWER

            Answered 2021-Apr-27 at 14:11

            features is just one string in one line of the file, not all the strings in that column.

            Add each word to the unique_list set in the loop, and print the set at the end.

            Source https://stackoverflow.com/questions/67275587

            QUESTION

            Adding hatches or patterns to ggplot bars
            Asked 2021-Apr-22 at 07:19

            Suppose I want to show in a barplot the gene expression results (logFC) based on RNA-seq and q-PCR analysis. My dataset looks like that:

            ...

            ANSWER

            Answered 2021-Apr-22 at 07:19

            Following the linked answer, it seems quite natural how to extend it to your case. In the example below, I'm using some dummy data structured like the head() data you gave, since the csv link gave me a 404.

            Source https://stackoverflow.com/questions/67164758

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

            Vulnerabilities

            No vulnerabilities reported

            Install rna

            You can install using 'npm i @ankumo/esbuild-plugin-html' or download it from GitHub, npm.

            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 .
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