tximport | summarize transcript-level estimates | Genomics library

 by   mikelove R Version: Current License: No License

kandi X-RAY | tximport Summary

kandi X-RAY | tximport Summary

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

Import and summarize transcript-level estimates for transcript- and gene-level analysis.
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              tximport has a low active ecosystem.
              It has 110 star(s) with 29 fork(s). There are 14 watchers for this library.
              OutlinedDot
              It had no major release in the last 6 months.
              There are 1 open issues and 40 have been closed. On average issues are closed in 51 days. There are no pull requests.
              It has a neutral sentiment in the developer community.
              The latest version of tximport is current.

            kandi-Quality Quality

              tximport has no bugs reported.

            kandi-Security Security

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

            kandi-License License

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

            kandi-Reuse Reuse

              tximport releases are not available. You will need to build from source code and install.

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            tximport Key Features

            No Key Features are available at this moment for tximport.

            tximport Examples and Code Snippets

            No Code Snippets are available at this moment for tximport.

            Community Discussions

            QUESTION

            Can a snakemake input rule be defined with different paths/wildcards
            Asked 2019-Jun-06 at 08:34

            I want to know if one can define a input rule that has dependencies on different wildcards.

            To elaborate, I am running this Snakemake pipeline on different fastq files using qsub which submits each job to a different node:

            1. fastqc on original fastq - no downstream dependency on other jobs
            2. adapter/quality trimming to generate trimmed fastq
            3. fastqc_after on trimmed fastq (output from step 2) and no downstream dependency
            4. star-rsem pipeline on trimmed fastq (output from step 2 above)
            5. rsem and tximport (output from step 4)
            6. Run multiqc

            MultiQC - https://multiqc.info/ - runs on the results folder which has results from fastqc, star, rsem, etc. However, because each job runs on a different node, sometimes Step 3 (fastqc and/or fastqc_after) is still running on the nodes while other steps finish running (Steps 2, 4 and 5) OR vice-versa.

            Currently, I can create a MultiQc rule which waits on results from Steps 2, 4, 5 because they are linked to each other by input/output rules.

            I have attached my pipeline as png to this post. Any suggestions would help.

            What I need: I want to create a "collating" step where I want MultiQC to wait till all steps (from 1 to 5) finish. In other words, using my attached png as guide, I want to define multiple input rules for MultiQC that also wait on results from fastqc

            Thanks in advance.

            Note: Based on comments I received from 'colin' and 'bli' after my original post, I have shared the code for the different rules here.

            Step 1 - fastqc

            ...

            ANSWER

            Answered 2019-Jun-06 at 08:34

            If you want rule multiqc to happen only after fastqc completed, you can add the output of fastqc to the input of multiqc:

            Source https://stackoverflow.com/questions/56450780

            QUESTION

            Extracting read counts matched to each gene symbol
            Asked 2019-Apr-10 at 12:45

            I have quantified gene expression by Salmon that gives me Ensembl transcripts, I converted Ensembl transcripts to gene symbol but for some genes I multiple transcripts; How I could collapse read counts to genes, I tried tximport package but I found that too hard as my annotation is different.

            ...

            ANSWER

            Answered 2019-Apr-10 at 12:45

            You can use the package dplyr.

            Create test table:

            Source https://stackoverflow.com/questions/55610723

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

            Vulnerabilities

            No vulnerabilities reported

            Install tximport

            You can download it from GitHub.

            Support

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            gh repo clone mikelove/tximport

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