Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • assemble RNAseq data with Oases but so many transcripts in locus_1

    Hello everyone

    I'm doing transcriptome assembly work with Oases.
    The illumina data's read length is 100nt and its quality is pretty good. I filterred bed reads, trimmed bases of low quality and trimmed adapters. Then did the Oases_pipeline in this command:
    Code:
    nohup oases_pipeline.py -m 17 -M 71 -s 2 -g 27 -o Hg0912 -d " -short Hg-trim.fasta " &
    The final result in transcripts.fa seems not so good. The first locus "locus_1" has so many transcripts, which exceeds 600,000.
    >Locus_1_Transcript_1/656445_Confidence_0.000_Length_257
    TTATTTTCTTCCTGTTGTTTTCAGTACGAGCCAGTTGAGATGCGCGTGAGTTTATAAACA
    AAACCTGTGTCCCCGATTGGCCAGTAAGTAGCCGGCAACCGACACGGACGTTGTACTTGT
    ATTGAGCAAAGTTTATTCCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACA
    TCCCGACGAATTGAGAACCTCTCCTTTTTGGGATAAAAAAAAAAAAAAAAAAAAAGTTGT
    ATTTTGTGTTTCAAAGT
    >Locus_1_Transcript_2/656445_Confidence_0.000_Length_505
    CATTCCTTGTATTCAAAAAAAAAAAAAAAAAAAAAAAAATGAAACACGTCAACAAAAAAA
    AAAAAAGGAACCCTTATTCTTAGAGAATTAAGACTTTTGCAAAAAAAAAAAAAAAAAAAA
    AAAAAAAAAAAAACATCCCGACGAATTGAGAACCTCTCCTTTTTGGGATAAAAAAAAAAA
    AAAAAAAAAAGCATGAAAAAAAAAAAATGCAGAAATCCCACTTTACTTTTAGATAAATAT
    TGCAAATTTGCGATACATAACATACATTAATTACATATAGGTAACTGTTTATTTTAAGGC
    AAATTCTTAGAAAAAACTAAGAAGTCCTGGATCAACTAAAAAATACAGCTCTCGAACGTC
    GCTCTTACAATTTTAAAACCAAGTTCCTTGAGTTAAAAATTGGAAAAAGTCGCGCTCGCT
    CCGCTCGCGATTTAGAAGCGATGTGCTTGTTTTTGCATTCGCCGGCCAACCAACAAAAAA
    TTATGGACGTTTGAGCTACACTTAT
    >Locus_1_Transcript_3/656445_Confidence_0.000_Length_407
    TCAAAAAAAAAAAAAAAAAAAAAAAAATGAAACACGTCAACAAAAAAAAAAAAAGGAACC
    CTTATTCTTAGAGAATTAAGACTTTTGCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAC
    ATCCCGACGAATTGAGAACCTCTCCTTTTTGGGATAAAAAAAAAAAAAAAAAAAAAGCAC
    GTCAACAAAAAAAAAAAAAGGAACCACATTGAATTTTGTGTTACGTCACTACTTTTAGGC
    ......
    And I pick out a long sequence to do blastx ,nothing similar found. But when blastn, the sequence can match to my species' genome sequences(my species do not have a complete genome sequneced, the matched subjects are something like BAC library).

    Is this normal?

  • #2
    Hi Minoru,

    I'm having the same problem. Did you find an answer for it? Thanks.

    Comment


    • #3
      Hi,
      Although our team has not seen this many transcripts under a given locus... what we have tended to do is set those loci with a given blastx hit as tier one transcripts (ie given them a higher ranking/priority over the other transcripts).

      On another note, not necessarily related to a scenario of the 6,000 transcripts under a single locus, but focussed on the results coming out of a transcriptome assembly: We found that the molecular biology protocols and depletions have a large impact on the resulting transcriptome assembly. In the early days before we had the protocols nailed down we found that a very large percent of our loci did not have blastx hits, as our molecular biology (ie not our bioinformatics) became more refined, we saw a much higher percent of loci matching to genes.

      I hope this is helpful.

      Jarret Glasscock
      Cofactor Genomics

      Comment


      • #4
        Thank you very much for the answer, it is very helpful.

        Mari

        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
        10 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