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Tutorial RNASeq for detection of pre-tumoral biomarkers using a group case study of Proliferative Verrucous Leukoplakia

  1. Página Principal
  2. Nuestros cursos
  3. RNASeq Leukoplakia
  4. 2.1.1 - Preparing your experiment
◄2. STEP-BY-STEP MODE TUTORIAL3. PIPELINE 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
  • 3. PIPELINE MODE TUTORIAL
    • 3.1 - TopHat/Hisat2 & Cufflinks protocol
  • 4. ACKNOWLEDGEMENTS
  • 5. BIBLIOGRAPHY
  • CITE US
  • 2.1.1 - Preparing your experiment

    When you have already downloaded the tutorial material, open RNASeq and set a directory folder to where you want the aforementioned material on your PC (e.g., your desktop). The space left of the directory browser is the FTP browser for RNAseq. This connects to the directory folder on your PC with your user account on the local host site of the server side. Right click in the FTP browser and create a folder named Tophat_cufflinks. Next, enter this folder and create the following subfolders:

    00_raw_data: folder to deposit the fastq files of both groups. If the fastq files are compressed, you must unzip them.

    01_quality_analysis: folder to deposit the results of the preprocessing analysis .

    02_preprocessed_reads: folder to deposit the results of the preprocessing analysis.

    03_refseq: folder to deposit the GRCh38.95 reference genome and its associated GTF.

    04_ mapping: folder to deposit for the results from mapping step.  

    05_transcriptome assembly: folder to deposit the results from the transcriptome assembly and quantification. 

    06_differential_expression: folder to deposit the results of the differential expression analysis.

    07_ go_enrichment_analysis: folder to deposit for the GO enrichment results from GOseq analysis.

    08_path_enrichment_analysis: folder to deposit for the pathway enrichment results from GOseq analysis. 

    Next, use the FTP browser to move the 15 fastq files under analysis from your PC directory browser to the folder 00_raw_data in your local host account on the server side. Then, use the FTP browser to move the GRCh38.95 reference genome, the GTF to folder 03_refseq, and the data sets needed for GO enrichment to folder 07_go_enrichment_analysis. Note that the procedure for enrichment of metabolic pathways using GOseq is exactly as performed for GOs but using the input material for metabolic enrichment previously indicated above. The whole process is shown in Video 1.

    Video 1. Setting directory folder and organizing the user account before starting 

    ◄2.1. - TOPHAT/HISAT2 & CUFFLINKS 2.1.2 - Quality analysis and preprocessing►
    • 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
      • 3. PIPELINE MODE TUTORIAL
      • 3.1 - TopHat/Hisat2 & Cufflinks protocol
      • 4. ACKNOWLEDGEMENTS
      • Pipeline mode: Tophat & Cufflinks protocol results
      • 5. BIBLIOGRAPHY
      • CITE US
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