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Tutorial RNASeq of comparative transcriptomics based on the species Sparus aurata

  1. Página Principal
  2. Nuestros cursos
  3. Tutorial RNASeq differential expression
  4. 3.2 - Mapping & Counting protocol
◄3. PIPELINE MODE TUTORIAL4. BIBLIOGRAPHY►
  • 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
  • 3.2 - Mapping & Counting protocol


    To complete this protocol using the pipeline mode, remember that you will need the following material:

    • The 5 fastq files of the infected group (samples from BI1 to BI5).
    • The 4 fastq files belonging to the control group (samples from BC1 to BC4).
    • The fasta file with the fSpaAur1.1 reference genome and its associated GTF file.
    • When you have this material ready, , you can access the pipeline designer interface (RNAseq Protocols → Pipeline mode) and proceed as indicated in video 13.


      Video 13. Mapping & counting protocol for differential expression analysis executed using the pipeline mode of RNASeq.


    Expected results from the Mapping & Counting protocol using the Pipeline execution mode:

    When the pipeline mode is completed, you will receive the results of differential expression sample with the reads mapped against the reference genome

    The expected results of this step are available in the following link Pipeline mode: Mapping & Counting protocol

    Remember you can check if the job was successfully completed by accessing the job tracking panel of RNASeq. 

    To learn more about any tool used in the pipeline and their outputs see their respective manuals, referred in previous sections of this tutorial.

    ◄3.1 - TopHat/Hisat2 & Cufflinks protocol4. BIBLIOGRAPHY►
    • Página Principal
    • Calendario
    • Secciones del curso
      • 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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