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Tutorial RNASeq of comparative transcriptomics based on the species Sparus aurata

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  3. Tutorial RNASeq differential expression
  4. 1.1 - Tutorial objective
◄1. PRELIMINARY INFORMATION2. STEP-BY-STEP MODE TUTORIAL►
  • CONTENTS
  • 1. PRELIMINARY INFORMATION
    • 1.1 - Tutorial objective
    • 1.2 - Tutorial material and case study
    • 1.3 - Experiment design and support
    • 1.4 - Installing and activating RNASeq and the Server-Side
  • 2. STEP-BY-STEP MODE TUTORIAL
    • 2.1. - TOPHAT/HISAT2 & CUFFLINKS
      • 2.1.1 - Preparing your experiment
      • 2.1.2 - Quality analysis and preprocessing
      • 2.1.3 - Mapping
      • 2.1.4 - Transcriptome Assembly
      • 2.1.5 - Differential Expression analysis
      • 2.1.6 - GOSeq
    • 2.2. - MAPPING & COUNTING PROTOCOL
      • 2.2.1 - Preparing your experiment
      • 2.2.2 - Quality analysis and preprocessing
      • 2.2.3 - Mapping
      • 2.2.4 - Postprocessing
      • 2.2.5 - Differential Expression analysis
  • 3. PIPELINE MODE TUTORIAL
    • 3.1 - TopHat/Hisat2 & Cufflinks protocol
    • 3.2 - Mapping & Counting protocol
  • 4. BIBLIOGRAPHY
  • CITE US
  • 1.1 - Tutorial objective


    The objective of this tutorial is to provide the end-user with the necessary training materials and information to manage server-side pipelines and workflows for differential expression analysis (DE) and enrichment in RNASeq and GPRO server side. The tutorial also provides a guideline to familiarize users with the two protocols and two execution modes of RNASeq as described below:

    Protocols: 

    • “Tophat/Hisat2 & Cufflinks” is recommended for DE studies when the reference genome has an annotation GTF/GFF file.  

    • “Mapping & Counting” is recommended for DE studies that do not have an associated GTF/GFF file.

    Execution modes:

    • Step-by-step mode: the protocol is executed as a workflow of independent steps (e.g. quality analysis, preprocessing, mapping, transcriptome assembly and/or quantification, differential expression, and enrichment) with each step shown in an separate tab. A scroll down bar is also provided for each step to summarizing the available command line interface (CLI) software for each step.  

    • Pipeline mode: all steps of the protocol are run automatically as a pipeline (i.e. one after another).

    For more details on the two protocols and the two execution modes, visit the manual for RNASeq at https://gpro.biotechvana.com/tool/RNAseq/manual/overview 

    ◄1. PRELIMINARY INFORMATION1.2 - Tutorial material and case study►
    • Home
    • Calendar
    • Course sections
      • CONTENTS
      • 1. PRELIMINARY INFORMATION
      • 1.1 - Tutorial objective
      • 1.2 - Tutorial material and case study
      • 1.3 - Experiment design and support
      • 1.4 - Installing and activating RNASeq and the Server-Side
      • 2. STEP-BY-STEP MODE TUTORIAL
      • 2.1. - TOPHAT/HISAT2 & CUFFLINKS
      • 2.1.1 - Preparing your experiment
      • 2.1.2 - Quality analysis and preprocessing
      • 2.1.3 - Mapping
      • 2.1.4 - Transcriptome Assembly
      • 2.1.5 - Differential Expression analysis
      • 2.1.6 - GOSeq
      • 2.2. - MAPPING & COUNTING PROTOCOL
      • 2.2.1 - Prepare your experiment for the mapping & counting analysis
      • 2.2.2 - Quality analysis and preprocessing
      • 2.2.3 - Mapping
      • 2.2.4 - Postprocessing
      • 2.2.5 - Differential Expression analysis
      • 3. PIPELINE MODE TUTORIAL
      • 3.1 - TopHat/Hisat2 & Cufflinks protocol
      • 3.2 - Mapping & Counting protocol
      • 4. BIBLIOGRAPHY
      • Pipeline mode: Tophat & Cufflinks protocol results
      • Pipeline mode: Mapping & Counting protocol results
      • CITE US
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