Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • fing
    Junior Member
    • Jun 2015
    • 1

    #1

    RNA seq analysis in R/BioConductor

    Hello,

    I am completely new to RNA seq data and have just received my first set of data. I research analysis options online in preparation and favoured the R/BioC setup due to my extensive previous experience in R more generally.

    The pipeline I have found instruction for is fairly simple:
    1. Alignment of reads to reference using QuasR
    2. Count reads
    3. Normalisation
    4. Identify differentially expressed genes
    ... with upstream analysis suggestions.

    My query is with the initial stages. There is not a separate stage of QC/cleaning, but my understanding of QuasR is that it produces a QC report with quality scores for each sample, and also a FastQ report with information on sample quality, proportion of bases, read lengths.

    Is this what is needed for QC before moving onto the next stage in the pipeline, or am I missing something? If I am missing something, any advice on where to look to complete the QC - especially in R/BioC! - would be very gratefully received.

    Thanks in advance to all!
  • westerman
    Rick Westerman
    • Jun 2008
    • 1104

    #2
    In general when mapping sequences to a known references (either genomic or transcriptome) there is no need for cleaning of the reads. They will map leaving the poor quality bases behind.

    For de-novo work cleaning does need to be done.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      Today, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM
    • SEQadmin2
      Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
      by SEQadmin2



      Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
      ...
      07-09-2026, 11:10 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Today, 02:55 AM
    0 responses
    8 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-23-2026, 11:41 AM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-20-2026, 11:10 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Working...