Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Pre processing of Illumina data

    Hi all!

    Though there have been many similar posts, but to have an updated (and more recent) thought, hence I am posting it again.

    I have some Illumina GAIIX paired end data in two separate files (with their suffix as _1 and _2). Before putting them for assembly, I need to perform certain pre processing of these file to alleviate its quality (probably FASTQ MASKER by quality control on GLAXY web tools). My query is " Should I join these paired end data first and then go on with the quality treatments OR should I just perform the quality treatment and then join the two files.

    Thanks in advance
    Any help will be deeply appreciated.

  • #2
    Originally posted by tusharbiot View Post
    My query is " Should I join these paired end data first and then go on with the quality treatments OR should I just perform the quality treatment and then join the two files.
    what do you mean when you say, "join"?

    Comment


    • #3
      With join I meant should I combine the two files into one (basically the tool I am using just concatenates the two sequences from a single locus/index).

      Comment


      • #4
        I know I didn't combine them during trimming based on qual...

        Comment


        • #5
          Originally posted by faozhi View Post
          I know I didn't combine them during trimming based on qual...
          faozhi, so that would mean you combined them after the quality screening.

          Comment


          • #6
            Originally posted by tusharbiot View Post
            Hi all!

            Though there have been many similar posts, but to have an updated (and more recent) thought, hence I am posting it again.

            I have some Illumina GAIIX paired end data in two separate files (with their suffix as _1 and _2). Before putting them for assembly, I need to perform certain pre processing of these file to alleviate its quality (probably FASTQ MASKER by quality control on GLAXY web tools). My query is " Should I join these paired end data first and then go on with the quality treatments OR should I just perform the quality treatment and then join the two files.

            Thanks in advance
            Any help will be deeply appreciated.
            It actually makes no difference at all, but you don't want to create extra work for yourself. With that in mind, you should probably trim the files separately, that way it will be easy to identify which read pairs were retained after the trimming and which reads should be treated as single-end.

            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...
              04-22-2024, 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, Today, 08:47 AM
            0 responses
            11 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            60 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            59 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            53 views
            0 likes
            Last Post seqadmin  
            Working...
            X