Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • BWA - read identity

    Hi,

    I'm using BWA to map my short sequencing reads (Illumina MiSeq) on a reference sequence. Is this possible to set the minimum % of identity with BWA? For exemple, if I set 90%, then all reads under this threshold will be discarded. I know the parameter "-n" can do something like this but the manual is not really clear (for me). Is "-n" the minimal absolute mismatch in term of base pairs?

    Thank you!

    Antony

  • #2
    Since nobody else has answered this, I will mention that I do not know of a way to generically do that in BWA. The manual says:
    -n NUM Maximum edit distance if the value is INT, or the fraction of missing alignments given 2% uniform base error rate if FLOAT. In the latter case, the maximum edit distance is automatically chosen for different read lengths. [0.04]
    ...which is clear in the case of int but unclear in the case of float. If all your reads are the same length you can calculate the edit distance that would correspond to that identity, though: e.g. 150bp * (1-0.90) = 15.

    Alternately, you can use BBMap, which has an "idfilter" flag - e.g. "idfilter=0.90", which will discard reads that don't map with at least 90% identity, regardless of their length. It also has an "idtag" flag, which will annotate all the alignments in the sam file with the percent identity, so you can manually filter them if you want.

    Comment


    • #3
      [This is a hack. I'm putting it here more for curiosity than anything else]

      On the aligned bam file you could capture the read length and the NM tag ("Edit distance to the reference, including ambiguous bases but excluding clipping") and print the alignment if L/NM < threshold. With samtools/awk:

      Code:
      samtools view -h aln.bam \
      | awk -v maxpct=0.05 -v OFS='\t' -v FS='\t' '{
          if($0 ~ /^@/){
              print $0
          } else {
              xnm=gensub(/.*\tNM:i:/, "", "g", $0); 
              nm=gensub(/\t.*/, "", "g", xnm); 
              pct=nm/length($10);
              if(pct < maxpct) {
                  print $0, "XP:f:"pct
              }
          }
      }' | less
      (The L/NM goes in tag XP)

      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...
        05-06-2024, 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, 05-07-2024, 06:57 AM
      0 responses
      12 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-06-2024, 07:17 AM
      0 responses
      16 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 05-02-2024, 08:06 AM
      0 responses
      22 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-30-2024, 12:17 PM
      0 responses
      24 views
      0 likes
      Last Post seqadmin  
      Working...
      X