Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • TopHat output and USCS genome browser question

    Hi folk! This is my first post and I'm quite new to next-gen sequencing analysis, so please be kind

    Here is some background on my data:
    mRNA from rat heart tissue was isolated and sequenced using a Heliscope from Helicos. I then converted the sms file generated by Helicos to a fasta file using a script in the Helisphere software. From there I used TopHat to look for splice junctions.

    From what I can see, everything went fine. The TopHat output includes all the files that I would expect it to include. Now, when I tried to view the .BED and .WIG files using the UCSC genome browser I have problems.

    Using the input found here --> http://genome.ucsc.edu/cgi-bin/hgGateway I tried to view my files after selecting genome->rat and the most recent assembly. I try to upload my .BED file and received the following error:
    "Error File 'junctions.bed' - Unrecognized format line 2 of custom track: gi|34868215|ref|NW_047355.1|Rn11_WGA1875_4 1124643 1138858 JUNC00000001 2 - 1124643 1138858 255,0,0 2 11,10 0,14205 (note: chrom names are case sensitive)"

    I am wondering if I'm even attempting to use the right tool to view the file or if there is some upstream problem?

    Any help would be appreciated.

    Thanks,
    Sam

  • #2
    The pre-built index for rat is built from NCBI contigs. In the first column of the bed file where it should be giving you a chromosome name you're getting the contig instead. You can build your own index from the UCSC fasta files with bowtie-build and it won't have this problem.

    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, Today, 06:35 AM
    0 responses
    12 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, Yesterday, 02:46 PM
    0 responses
    18 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-07-2024, 06:57 AM
    0 responses
    17 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 05-06-2024, 07:17 AM
    0 responses
    19 views
    0 likes
    Last Post seqadmin  
    Working...
    X