Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Forward-reverse read counts don't match

    This is 16S metagenomic seq data, sent to service provider for MiSeq but they did HiSeq and 1/16th lane, 300 PE.
    However, now CLC Workbench is flagging at the import paired-end read stage, saying:
    "The data seems to be corrupt or originates from different sources since the input files contain different numbers of reads! The previous sequences have been properly saved but it is highly likely the import data is incomplete or defect. Please double-check the sources."
    There seems to uneven number of forward and reverse reads:
    2279992 A1.1.fq
    1924508 A1.2.fq
    463012 A2.1.fq
    389656 A2.2.fq
    Is this normal, how serious is the flag posted? How am I to ensure that forward and reverse reads really in pairs?

  • #2
    Sounds like your core may have trimmed data using BaseSpace (or some other means) which left orphan reads (they did not do PE aware trimming). You should ask them to provide raw/untrimmed original data.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      Yesterday, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    52 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    45 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X