Transpi
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The use of RNA-Seq data and the generation of de novo transcriptome assemblies have been pivotal for studies in ecology and evolution. This is distinctly true for non-model organisms, where no genome information is available. Nevertheless, studies of differential gene expression, DNA enrichment baits design, and phylogenetics can all be accomplished with the data gathered at the transcriptomic level. Multiple tools are available for transcriptome assembly, however, no single tool can provide the best assembly for all datasets. Therefore, a multi assembler approach, followed by a reduction step, is often sought to generate an improved representation of the assembly.
Transpi
TransPi provides a useful resource for the generation of de novo transcriptome assemblies, with minimum user input but without losing the ability of a thorough analysis. TransPi requires various databases to run. The precheck script will installed the databases and software, if necessary, to run the tool. The precheck run needs a PATH as an argument for installing locally all the databases the pipeline needs. Once the precheck run is done it will create a file named nextflow. If selected, it will also have the local conda environment PATH. The nextflow. We recommend to run TransPi with the option --all where it will do the complete analysis, from raw reads filtering to annotation. Other options described below. If you combined multiple libraries of the same individual to create a reference transcriptome, which will be later use in downstream analyses e. Differential Expression , make sure the kmer list is based on the length for the shortest read library and the maxReadLen based on the longest read length. TransPi can also use docker, singularity, and individual conda installations i. Refer to Section 6 of this manual for further details on deployment of TransPi using other profiles.
It took years until the first widely accepted set transpi benchmarks beyond raw statistical evaluation became available e. The interactive report at the end of the pipeline is also a significant advantage for us, researchers, who want to check our assembly's quality quickly before going to the next steps of the project. The article presents a meta transpi to transcriptome assembly, transpi, validation, and annotation.
TransPi is based on the scientific workflow manager Nextflow. It is designed to help researchers get the best reference transcriptome assembly for their organisms of interest. It performs multiple assemblies with different parameters to then get a non-redundant consensus assembly. All these with minimum input from the user but without losing the potential of a comprehensive analysis. Figure 1. TransPi v1.
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community. Already on GitHub? Sign in to your account. After exhaustive troubleshooting, it seems the condaEnv that contains BUSCO is not being activated during the execution of the pipeline. I am using the versions: Nextflow version Any thoughts?
Transpi
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community. Already on GitHub? Sign in to your account. I have an issue with trying to run Full Analysis on TransPi. Everything was downloaded and installed without any error. I tried to use the full analysis by running "nextflow run TransPi. Something went wrong.
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Compared to approaches using single assemblers only, TransPi produces higher BUSCO completeness percentages, and a concurrent significant reduction in duplication rates. This process may take a while depending on the options you select. Default "false" --skipKegg Skip kegg analysis. You switched accounts on another tab or window. Carpool Kids: Family Calendar. TransPi is easy to configure and can be deployed seamlessly using Conda, Docker and Singularity. A directory called work is also created when running TransPi. To minimize pickup and drop-off time, and make you comfortable during the ride. It is designed to help researchers get the best reference transcriptome assembly for their organisms of interest. Therefore, a multi assembler approach, followed by a reduction step, is often sought to generate an improved representation of the assembly. One of the main advantages of this approach is its flexibility in working on data from both "model" and "non-model" organisms and various levels of user expertise. However, an approach to find the right balance between the number of transcripts or isoforms vs. Cite this recommendation as: Simakov, O. However the original HTML file with interactive visualization i. TransPi is easy to configure and can be deployed seamlessly using Conda, Docker and Singularity.
TransPi is based on the scientific workflow manager Nextflow.
Docker or singularity can also be use for deploying TransPi. It expects one file per sample to perform the annotation. TransPi is easy to configure and can be deployed seamlessly using Conda, Docker and Singularity. Thus we have custom profiles for the submission of jobs. Other parameters --minQual Minimum quality score for fastp filtering. The use of RNA-Seq data and the generation of de novo transcriptome assemblies have been pivotal for studies in ecology and evolution. Also, your captain will be matched from a near location with you. This led to many studies using a custom set of tools with ensuing various degrees of reproducibility. The line clusterOptions can be used to add any other option that you will usually use for your job submission. You can do multiple transcriptomes at the same time. TransPi can also use docker, singularity, and individual conda installations i. Full run and extra annotation Scenario:. Example: -profile test,singularity. TransPi provides a useful resource for the generation of de novo transcriptome assemblies, with minimum user input but without losing the ability of a thorough analysis.
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