Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • frankyue50
    Member
    • Nov 2008
    • 34

    tophat strand info?

    can anyone help me identify if the strand info is in the accepted.sam file (tophat output)
    SOLEXA1_0001:1:60:7595:15462#0 16 chr1 3000555 255 36M * 0 0 AATTTGTTTTGTCCTTCAGCGGATTAAAATATTCAG CBBBCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC NM:i:0

    or does anyone know what is column 2 and 4 means. I checked sam manual but still confused. Thanks.
  • john_mu
    Member
    • May 2010
    • 88

    #2
    Hi,

    The strand info will only be on the junction reads. It is impossible to determine the strand of non-junction hits without using a stranded protocol in the experiment.

    column 2 is the SAM flag. You can google "SAM flag" to find out.

    column 4 is the chromosome start location of the hit.
    SpliceMap: De novo detection of splice junctions from RNA-seq
    Download SpliceMap Comment here

    Comment

    • smueller
      Junior Member
      • Mar 2011
      • 1

      #3
      Hey,

      I just came accross the same problem and found that you can read strand info from the
      2nd colunmn. This is actually a flag that has to be deciphered according to the SAM format and can be done for instance here:

      In your case, 16 means that this read is on the reverse strand.
      Column 4 is the start postition of this read on the respective chromosome.
      Note, since tophat produce BAM formats as default for a while, you can still
      access the flag information with:
      samtools view accepted_hits.bam
      which produces SAM format.

      cheers
      Sebastian

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM
      • 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...
        07-08-2026, 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 07-13-2026, 10:26 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-09-2026, 10:04 AM
      0 responses
      30 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-08-2026, 10:08 AM
      0 responses
      18 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-07-2026, 11:05 AM
      0 responses
      34 views
      0 reactions
      Last Post SEQadmin2  
      Working...