Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • lfaino
    Junior Member
    • Mar 2011
    • 9

    RNA-seq assembly

    Dear All,
    I did an RNA-seq by using Illumina and now i would like to assemble it. I already used velvet and I got some nice results. However the assembly is not good enough. In NCBI there are some related species that are sequenced and I could give a try in assemble the RNA-seq data with these genomes. Can you suggest some software that I can use? As a input file, I have a FASTQ file.

    Thanks

    Luigi
  • edge
    Senior Member
    • Sep 2009
    • 199

    #2
    Hi Ifaino,

    I'm dealing with RNA-seq as well.
    Can I know how you identify whether the assemble result is good or not?
    I'm plan to use MIRA for my RNA-seq de novo assembly.
    Thanks for your sharing.

    Comment

    • lfaino
      Junior Member
      • Mar 2011
      • 9

      #3
      Hi edge,
      I know because a lot of assembled transcripts are not complete when I BLAST them against genomes of related species. Just for this. And for this reason. I would like to assemble my transcriptome against a reference genome.

      Luigi

      Comment

      Latest Articles

      Collapse

      • GATTACAT
        Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by GATTACAT
        Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
        07-01-2026, 11:43 AM
      • SEQadmin2
        Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by SEQadmin2


        I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

        Here are nine questions we think about, in roughly the order they matter, before...
        06-18-2026, 07:11 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 11:08 AM
      0 responses
      6 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-30-2026, 05:37 AM
      0 responses
      11 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-26-2026, 11:10 AM
      0 responses
      19 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      53 views
      0 reactions
      Last Post SEQadmin2  
      Working...