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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. 2.2. - MAPPING & COUNTING PROTOCOL
◄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
    • 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
  • 2.2. - MAPPING & COUNTING PROTOCOL

    The current protocol (Mapping & Counting) differs from the Tophat/Hisat2 & Cufflinks protocol in that transcripts are counted to quantify the expression patterns and both the mapping, and the differential expression analysis, are performed without a GTF/GFF file. To complete the tutorial via the mapping & counting protocol, we use the 9 fastq files (BI1 to BI5 and BC1 to BC4) as well as the RefSeq fasta file with the transcripts of the fSpaAur1.1 release. In this this tutorial we will use a transcriptome data set as reference instead of the genome because we are not going to use the GTF file.


    ◄2.1.6 - GOSeq2.2.1 - Prepare your experiment for the mapping & counting analysis►
    • 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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