Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • thejustpark
    Member
    • Jul 2012
    • 28

    Do you guys know how to use net file format?

    Hello experts,

    I am trying to obtain human genes that overlap my mouse lncRNAs in human-mouse pairwise alignment.
    For this purpose, I have been looking at mouse-human pairwise alignment in net format, but I can't fully understand what to do.

    Is there no tool that can take in a net-formatted pairwise alignment and a bed file with genes of my interest in one species and spit out their counterparts for the other species based on the net file? I thought there should be such tools, but couldn't find one. And now I can't believe there is none for this purpose.

    If you know how to do this, or know of tools for this, please let me know.

    Thanks,
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    I have no clue what the "net" format is, you'd need to provide a link. The easier route would be to make a GTF file of mouse lncRNAs and then use liftOver (or the online version from UCSC) to convert those to human coordinates. Then you have a single coordinate system to work and can simply subset your human annotation file with whatever tools you want (I'd suggest making a GRanges object in R out of things and just using its subset functions...that'd be quick and easy enough).

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Cancer Drug Resistance: The Lingering Barrier to Rising Survival
      by SEQadmin2



      Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

      There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
      Today, 05:17 AM
    • 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, Today, 10:08 AM
    0 responses
    6 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 11:05 AM
    0 responses
    7 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-02-2026, 11:08 AM
    0 responses
    30 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-30-2026, 05:37 AM
    0 responses
    28 views
    0 reactions
    Last Post SEQadmin2  
    Working...