Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • slowsmile
    Member
    • May 2011
    • 22

    #1

    Can Pindel applied to SOLiD data?

    Dear All
    Just want to know if anyone has relevant experiences in calling INDELS using Pindel on SOLiD data. We used Pindel on Illumina samples (bam files) with good outcome but now when we moved to SOLid data (bam files, already mapped to reference genome), all I got are empty output files

    I have very little experience with SOLiD data, can anyone share with me your experience in applying Pindel to SOLiD data? What procedure did u go through to get the results?
    Thanks
  • KaiYe
    Senior Member
    • Jun 2009
    • 133

    #2
    Originally posted by slowsmile View Post
    Dear All
    Just want to know if anyone has relevant experiences in calling INDELS using Pindel on SOLiD data. We used Pindel on Illumina samples (bam files) with good outcome but now when we moved to SOLid data (bam files, already mapped to reference genome), all I got are empty output files

    I have very little experience with SOLiD data, can anyone share with me your experience in applying Pindel to SOLiD data? What procedure did u go through to get the results?
    Thanks
    Pindel expects the read orientation as in Illumina paired-end. There is one sam2pindel program to handle SOLiD data but performance is not guaranteed to be optimal.

    Comment

    • slowsmile
      Member
      • May 2011
      • 22

      #3
      Thanks Kaiye for your suggestion

      However, I am still unable to convert the SoLID bam files into Pindel compatible format with the sam2pindel function. The reads in my SoLID bam file looks like this:

      475_151_1990 0 chr1 10108 38 72M3H * 0 0 CAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCCTAACCCTAACCCTAACCCTNNCCCTAACC AAA@@>@AAA@??@@@??@?@@??>>>=<<=>>>==>>>>===>>>>==>>>>==>5440'-7710576888 BD:Z:SSTSYVXWVVVRTSRSTQSRQRSPSRQRSPSRQRSPSRQRSPPSRQRSPSRQRSPRQPRSPSRSTUTWSRST PG:Z:MarkDuplicates RG:Z:ugc_509_10_10 NH:i:50 BI:Z:VVUVYWZXVWVSUUTVVTWUTUVSWTTUVTWTTVVTVTSUUSSVTSUUSVTSUUSVTRSSRTWYYYWZUTVV CM:i:1 NM:i:0 CQ:Z:@@>@@@@@@@@@@@@@@@@@@@?@??6@>@;8=>;?/2/66622/2<836/2222;//<82</6/82//22@>8/ CS:Z:T210100230100230100230100230100230100230100023010023010023010022010023010023
      407_312_991 0 chr1 10140 2 39M36H * 0 0 ACCCTAACCCCTAACCCTAACCCTAACCCTAACCCTAAC AA@?A?@A@@@@?@@??@@?@??@>>><<==>>==>>2+ BD:Z:SSTQYXVWXTSUSRSTQTRQRSPSRQRSPSRQRSPTSRS PG:Z:MarkDuplicates RG:Z:ugc_509_10_10 NH:i:50 BI:Z:VVVTZXWYXUTVSTVVTWUTVUTVUSVUTWUSVVTWUTV CM:i:0 NM:i:0 CQ:Z:@@@@@@@@@@@2=68@@66>2@@/@<8@@8<@/2@/62/28/2/////<68/;//62////////;2///2/88= CS:Z:T310023010002301002301002301002301002301100300103330103330300133112133002133
      I tried "samtools view -h input.bam | ./sam2pindel - output.pindel 250 sample 0"
      and the output "output.pindel" contain 0 reads somehow

      I even tried the newer version of sam2pindel with the "Illumina-PairEnd" at the end, it still generates 0 reads in the output file

      Any suggestion?
      Thank you

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        07-31-2026, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 08-13-2026, 12:22 PM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      32 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      50 views
      0 reactions
      Last Post SEQadmin2  
      Working...