Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • evakoe
    Member
    • Jul 2012
    • 27

    #1

    HLA typing with bwakit

    Dear all,

    has somebody attempted HLA typing with bwakit and can share some experience?
    I have whole exome sequencing data of human individuals for who I would like to do HLA typing. I ran the bwakit as instructed in the Readme, but have problems interpreting the output. Here are the first few lines from the out.hla.all for HLA-B for one individual.
    Code:
    HLA-B*50:01:01  HLA-B*55:01:01  0       0       2
    HLA-B*50:01:02  HLA-B*55:01:01  0       0       2
    HLA-B*50:01:04  HLA-B*55:01:01  0       0       2
    HLA-B*50:01:01  HLA-B*55:01:03  0       0       2
    HLA-B*50:01:02  HLA-B*55:01:03  0       0       2
    HLA-B*50:01:04  HLA-B*55:01:03  0       0       2
    HLA-B*50:01:01  HLA-B*55:01:07  0       0       2
    HLA-B*50:01:02  HLA-B*55:01:07  0       0       2
    HLA-B*50:01:04  HLA-B*55:01:07  0       0       2
    Here Heng Li explains the meaning of columns 3 to 5:
    column 3: #mismatches on the primary exon(s)
    column 4: #mismatches on all considered exons
    column 5: #exons used in typing

    My questions are:
    1. What are columns 1 and 2? I would have expected results for one allele, not two.
    2. What is the "best" or the "true" allele? The out.hla.top file simply gives the first line of the out.hla.all for each gene, but from the evidence in the out.hla.all file, the first line does not seem to be better than the second or third.
    3. Would you say that given high coverage exome sequencing data, one should be able to clearly identify (with bwakit) the true allele an individual has for each of the HLA genes?

    Thank you
    Eva
    Last edited by evakoe; 05-08-2017, 06:08 AM.
  • evakoe
    Member
    • Jul 2012
    • 27

    #2
    For the people interested in this post:
    1. I assume the first two columns are the HLA alleles for the two human alleles, so the HLA-B allele is heterozygous in this case.
    2. The coverage was probably not high enough to determine a six digit resolution. After all, the first four digits are allthe same, and the last two are variable. I ran OptiType on the same sample which gave the output
    Code:
    B1	B2
    B*50:01	B*55:01
    3. The coverage on this sample is about 25X, which apparently is enough for four digit resolution with bwakit, but not for six digit resolution.
    Last edited by evakoe; 05-17-2017, 02:51 AM.

    Comment

    • afadda
      Member
      • Jun 2010
      • 15

      #3
      hi evakoe,

      which command did you use? cuz i'm trying to do the same but it's not working.
      i'm using this:
      run-bwamem -o NA12878-hs38 -t 20 -H -s /gpfs/data_jrnas1/ref_data/Hsapiens/hs38DH/hs38DH.fa NA12878_2.fastq.gz NA12878_1.fastq.gz |sh
      and it doesn't give me sorted bam or HLA typing.

      Comment

      • evakoe
        Member
        • Jul 2012
        • 27

        #4
        The command I used was
        Code:
        run-bwamem -t 4 -R "@RG\tID:myID\tSM:mySM\tPL:myPL\tLB:myLB\tPU:myPU" -H -d -s -o sample BWAindex sample_1.fastq sample_2.fastq | sh
        and it ran as expected

        Comment

        Latest Articles

        Collapse

        • 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
          ...
          Yesterday, 10:25 AM
        • SEQadmin2
          How Immunogenomics Decodes Immunity’s Genetic Blueprint
          by SEQadmin2




          The immune system’s power comes from its genetic diversity, allowing myriad threats to be neutralized through first recognizing foreign antigens. That diversity is also what makes the immune system so difficult to study. Recent advances in sequencing technology and computational biology, however, are giving researchers new tools to understand immune responses and immune-related diseases in greater detail.

          This convergence of genetics, immunology, and computation...
          09-01-2026, 05:41 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 09-25-2026, 09:06 AM
        0 responses
        30 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 09-23-2026, 11:05 AM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 09-18-2026, 11:37 AM
        1 response
        46 views
        0 reactions
        Last Post pekgio
        by pekgio
         
        Started by SEQadmin2, 09-16-2026, 10:23 AM
        1 response
        55 views
        0 reactions
        Last Post pekgio
        by pekgio
         
        Working...