Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Danko1
    Junior Member
    • Mar 2014
    • 6

    Extract consensus from BAM + fill gaps from reference

    Hi everyone!

    I am new to this forum and have the following question:

    How can I extract the consensus sequence from a BAM alignment AND fill positions where there might be gaps in the alignment with the reference sequence from the alignment?

    I know that there is a way using samtools mpileup to extract a consensus sequence from a BAM file but the "fill from reference" option is very important to me.

    Any ideas what tools I could use to easily extract the consensus this way?

    Thanks for your help!
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Quoting from one of the samtools pages:

    Code:
    samtools mpileup -uf ref.fa aln.bam | bcftools view -cg - | vcfutils.pl vcf2fq > cns.fq

    Comment

    • Danko1
      Junior Member
      • Mar 2014
      • 6

      #3
      Thanks for your quick answer dpryan!

      I know this samtools code, but this won't allow to fill gaps in the alignment with the reference sequence of the alignment at that position so that I end up with a consensus fasta file without any gaps, right?

      How can I extract the consensus sequence from an alignment where positions where there are gaps are filled with the corresponding nucleotide(s) from the reference sequence of the alignment?

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        That actually should produce a consensus file. At least the output from bcftools will contain the SNP calls for every base and the reference sequence (regardless of whether the base is covered or not), so if that's not working correctly then presumably there's been a change in vcfutils.pl. To confirm this, what happens if you:

        Code:
        samtools mpileup -uf ref.fa aln.bam | bcftools view -cg - >foo.vcf
        and then look at one of the gaps? It should be covered in the VCF (if not, then I likely mistyped something). The only trick then is converting the reference given the VCF file, which which there are other options (GATK has a tool for that).

        Comment

        • Danko1
          Junior Member
          • Mar 2014
          • 6

          #5
          So I tested the proposed code to generate a consensus from a BAM alignment:

          samtools mpileup -uf ref.fa aln.bam | bcftools view -cg - | vcfutils.pl vcf2fq > cns.fq

          It works fine, despite the fact that I end up with 'N' at every position where my reads don't map to the reference in the alignment.

          How can I replace those 'N's' by the original nucleotides from the reference at this position? I am glad for any help!

          @dpryan: Did you mean the FastaAlternateReferenceMaker by GATK? Have you used this tool before?

          Comment

          • Danko1
            Junior Member
            • Mar 2014
            • 6

            #6
            Figured it out! The GATK tool did the trick! Thanks for your help!

            Comment

            Latest Articles

            Collapse

            • 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
            • SEQadmin2
              Nine Things a Sample Prep Scientist Thinks About Before Sequencing
              by SEQadmin2


              I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

              Here are nine questions we think about, in roughly the order they matter, before...
              06-18-2026, 07:11 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 07-02-2026, 11:08 AM
            0 responses
            16 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-30-2026, 05:37 AM
            0 responses
            17 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-26-2026, 11:10 AM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            54 views
            0 reactions
            Last Post SEQadmin2  
            Working...