Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • from gene coverage to sex determination

    Hello everybody

    I am interested in determining sex from my nextseq runs. I read somewhere that a possibility is to calculate gene coverage for X and Y genes and then do sex determination

    if cov(x)> cov(y) -> XX
    if cov(x)~=cov(y) -> XY

    to determine X coverage in Linux I am using samtools

    samtools view <file.bam> RNAME 'chr[XY]'|wc -l

    and the data I'm getting looks like

    paumarc@bioinf[refSamples] samtools view wtsorted.bam RNAME 'chrY'|wc -l [ 4:39]
    [main_samview] region "RNAME" specifies an unknown reference name. Continue anyway.
    93504
    paumarc@bioinf[refSamples] samtools view wtsorted.bam RNAME 'chrX'|wc -l [ 4:39]
    [main_samview] region "RNAME" specifies an unknown reference name. Continue anyway.
    1020263

    The question is: Can I determinate sex only with this or i should do some kind of correction? it is normal to have more reads on chrx as long as it is bigger)

    thanks

    pau
    Last edited by paumarc; 10-09-2015, 06:44 AM.

  • #2
    You'll definitely need to correct for the difference in size (Y is much smaller than X), but they may have differences in mappability as well. I would encourage you to look at a few samples for which you know the gender and that'll give you some decent numbers to start with.

    BTW, "samtools view -c foo.bam chrX" will be faster than piping to "wc -l".

    Comment


    • #3
      With samtools idxstats you'll get the result even faster plus the length of the chromosomes.

      Since you may get mapping artefacts from intron regions, you can use a bed-file of known (chrY / chrX) - genes to limit your look-up:
      Code:
      samtools view -c -L chrX-genes.bed foo.bam 
      samtools view -c -L chrY-genes.bed foo.bam
      The result should be corrected, as Devon posted.

      BTW.: in your command you use the keyword RNAME; this is not necassary.

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM
      • seqadmin
        Strategies for Sequencing Challenging Samples
        by seqadmin


        Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
        03-22-2024, 06:39 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      25 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      24 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      52 views
      0 likes
      Last Post seqadmin  
      Working...
      X