Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dietmar13
    Senior Member
    • Mar 2010
    • 107

    #1

    Annotation of small RNA seq data?

    hi,

    i have small RNA seq data from ~ 50 isolated tumor cell samples (~700 mio reads) and found at least 1282 new miRNAs (predicted by two independent methods and supported by at least 100 reads) and thousands (>150 k !!!) of nc transcripts (no annotation known) also supported by >100 reads.

    short outline of the analysis so far:
    filter quality, remove adaptor, keep complete small RNAs between 13-37 nt
    predict new miRNAs with mirDeep_star and nc transcripts with NorahDesk.

    consolidate new miRNAs (from mirDeep_star) and use mirBase v20, gencode 19 annotation and a few other annotations (e.g. piwiRNAs) and the new found miRNAs to annotate the NorahDesk nc transcripts. but most of them left un-annotated.

    finally, i mapped all 13-37 nt reads to these nc transcripts (stringent) and summed the reads for each sample and nc-transcript.

    I wanted to ask you what kind of annotation could be done with these nc transcripts. is there a good method to estimate e.g. conservation among vertebrates (which degree? familiy, class, phylum, ... would be useful).

    what else could be done - the small RNA transcriptome seems to be very complex?

    best,

    dietmar

Latest Articles

Collapse

  • SEQadmin2
    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
    by SEQadmin2



    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
    ...
    10-14-2026, 09:55 AM
  • SEQadmin2
    New Genomics Technologies Take Aim at Long-Standing Limits
    by SEQadmin2


    Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

    We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
    ...
    09-28-2026, 10:25 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 10-22-2026, 11:13 AM
0 responses
60 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-22-2026, 10:48 AM
0 responses
42 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-15-2026, 10:52 AM
0 responses
57 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 10-14-2026, 05:39 AM
0 responses
61 views
0 reactions
Last Post SEQadmin2  
Working...