Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Samtools mpileup error "[W::sam_read1] parse error at line 1"

    Hello everyone,

    I am analyzing WGS data of my mutant (Raw data in fastq), I performed the alignment by using Bowtie and BWA as:

    Using Bowtie:
    bowtie -S reference.fa file.sam
    then converted the sam file to bam file
    samtools view -bS -o file.bam file.sam

    Using BWA:
    bwa aln reference.fa file.fastq > file.sai
    bwa samse reference.fa file.sai file.fastq gzip > file.sam.gz

    then converted sam.gz to bam
    samtools view -bt reference.fa file.sam.gz | samtools sort -o file.bam

    Then I tried to use mpileup on both bam files but got similar errors:

    samtools mpileup -v reference.fa file.bam > outfile

    [mpileup] 2 samples in 2 input files
    <mpileup> Set max per-file depth to 4000
    [W::sam_read1] parse error at line 1

    Can anyone explain whats wrong and how it can be corrected?
    Thanks

  • #2
    Check samtools mpileup man page.
    You may want to try -f instead of -v ?

    Comment


    • #3
      Are you using the newest versions of bwa/samtools?

      Comment


      • #4
        @dschika will it then give vcf format output?

        @GenoMax,

        I am using bwa-0.7.13 and
        samtools-1.3

        Comment


        • #5
          Ok, probably you want to use -v and -f, my bad.

          As you read the manual which you can find here, you know what -v and -f do:

          -f, --fasta-ref FILE The faidx-indexed reference file in the FASTA format. The file can be optionally compressed by bgzip.
          -v, --VCF Compute genotype likelihoods and output them in the variant call format (VCF). Output is bgzip-compressed VCF unless -u option is set.

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Recent Advances in Sequencing Analysis Tools
            by seqadmin


            The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
            Today, 07:48 AM
          • seqadmin
            Essential Discoveries and Tools in Epitranscriptomics
            by seqadmin




            The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
            04-22-2024, 07:01 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, Today, 07:17 AM
          0 responses
          11 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 05-02-2024, 08:06 AM
          0 responses
          19 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-30-2024, 12:17 PM
          0 responses
          20 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-29-2024, 10:49 AM
          0 responses
          28 views
          0 likes
          Last Post seqadmin  
          Working...
          X