Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • kevinrue
    Member
    • Jan 2013
    • 25

    #1

    HISAT2 / hisat2_extract_snps_haplotypes_VCF.py: only first variant in output

    Dear all,

    I am trying to apply the hisat2_extract_snps_haplotypes_VCF.py script to merged VCF files: one file per human chromosome, all files contains genotypes for the same set of samples.

    A typical command I run is:

    hisat2_extract_snps_haplotypes_VCF.py --non-rs --verbose /scratch/genomes/grch37/84/fasta/Homo_sapiens.GRCh37.dna.primary_assembly.fa vcf/chr14_PASS_vep.vcf.gz HiSat2/extract/chr14_PASS_vep

    Facts:
    • The script typically take between 20min and 2h20min depending on the chromosome length.
    • However, the output SNP and haplotype files both contain a single line (i.e. variant). I compared, and each time it is the first variant in the VCF file processed.
    • I do not see any error or output message , despite the --verbose option.
    • Considering the run time, it seems that the script is processing all variants, just not outputting anything after the first variant


    Is there some aspect of my VCF files that I should check for compatibility with the script?

    Many thanks in advance.

    Kevin
  • kevinrue
    Member
    • Jan 2013
    • 25

    #2
    Problem identified (not solved)

    Got it!

    I drilled down into the code of (hisat2_extract_snps_haplotypes_VCF.py)
    and found the following bit of code that ignores variants with duplicated ID (3rd column).

    Code:
    if varID == prev_varID:
        continue
    In my case, the VCF was generated from WGS, and variants are not yet annotated with any RSID (existing or novel).
    As a result they all have ID ".", and leads the code above to skip all variants after the first one (and explains why the script still runs with a time proportional to the chromosome length, as it does properly scan all variants in the VCF file).

    My solution:
    I'll just build a genome index using the UCSC snp146Common.txt file (as the current pre-built index available on the HISAT website seems to be based on dbSNP 144)

    Any comment welcome!
    Kevin

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
      by SEQadmin2




      NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
      10-30-2026, 06:46 AM
    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      10-14-2026, 09:55 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 10-28-2026, 09:57 AM
    0 responses
    40 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-28-2026, 09:51 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 11:13 AM
    0 responses
    73 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    48 views
    0 reactions
    Last Post SEQadmin2  
    Working...