Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Question about trimmomatic

    Hi,

    I'm a first time user to trimmomatic and I have paired-end RNA seq data. My question why do I get paired and unpaired output for each read at the output?

    java -classpath <path to trimmomatic jar> org.usadellab.trimmomatic.TrimmomaticPE [-threads <threads>] [-phred33 | -phred64] [-trimlog <logFile>] <input 1> <input 2> <paired output 1> <unpaired output 1> <paired output 2> <unpaired output 2> <step 1>

    I have used CLC genomics for trimming and using that I'll get two output files namely read1_trimmed.fastq and read2_trimmed.fastq. Why do I get 4 output files in trimmmomatic?

  • #2
    I got the answer from Federico.

    the answer is: because Trimmomatic doesn't discard unpaired reads, as CLC does.
    Trimmomatic trims both reads in a pair. If one of the reads is of high quality, and the second one is of low quality, only the first is kept. This may happen in cases when the two sequencing cycle groups have generally different noise levels (recently, it happened in our institute that the laser died during the second cycle, and trimming removed most of the _2 reads, allowing us to keep the _1).

    Most of the other non-CLC trimming tools do the same as Trimmomatic. If you really don't want them, you can ignore _U1 and _U2. Trimmomatic just give you an extra chance to use your unpaired sequences.

    Federico

    Comment


    • #3
      For assembly which reads should be used? paired one or unpaired...

      Comment


      • #4
        Originally posted by Rahul shelke View Post
        For assembly which reads should be used? paired one or unpaired...
        You can use both. Depends on the assembler.

        Comment


        • #5
          Hi everybody,

          Just joined the forum, hope you're still following the thread.

          To keep on the subject, is it possible to assemble both datasets (paired+unpaired) in order to perform an assembly (Trinity) and not lose precious data.

          Thanks

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Recent Advances in Sequencing Analysis Tools
            by seqadmin


            The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
            05-06-2024, 07:48 AM
          • 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

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Yesterday, 06:57 AM
          0 responses
          12 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-06-2024, 07:17 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-02-2024, 08:06 AM
          0 responses
          19 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-30-2024, 12:17 PM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Working...
          X