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
              Best Practices for Single-Cell Sequencing Analysis
              by seqadmin



              While isolating and preparing single cells for sequencing was historically the bottleneck, recent technological advancements have shifted the challenge to data analysis. This highlights the rapidly evolving nature of single-cell sequencing. The inherent complexity of single-cell analysis has intensified with the surge in data volume and the incorporation of diverse and more complex datasets. This article explores the challenges in analysis, examines common pitfalls, offers...
              06-06-2024, 07:15 AM
            • seqadmin
              Latest Developments in Precision Medicine
              by seqadmin



              Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

              Somatic Genomics
              “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
              05-24-2024, 01:16 PM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 06-07-2024, 06:58 AM
            0 responses
            13 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 06-06-2024, 08:18 AM
            0 responses
            20 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 06-06-2024, 08:04 AM
            0 responses
            18 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 06-03-2024, 06:55 AM
            0 responses
            13 views
            0 likes
            Last Post seqadmin  
            Working...
            X