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BBMAP outputs multimapped reads in ambiguous=toss

Hi,

I aligned some dna-seq paired-end data using bbmap. I want to filter out the multi-mapped reads thus I used the ambiguous=toss parameter. However when I checked my alignment file in IGV I found some reads aligning on regions that are found multiple times in the genome (hg19). Here's the command I used :

bbmap.sh path=$bbmapHost local=t ambiguous=toss in1=R1.fastq in2=R2.fastq threads=1 minid=0.90 maxindel=1 mappedonly=t overwrite=t pairedonly=t sam=1.3 out=out.sam

Is there something wrong ?

Here's an example :

BLAT on the highlighted sequence in IGV shows multiple identical regions in the human genome :
http://grch37.ensembl.org/Homo_sapiens/Tools/Blast/Results?db=core;tl=gyu9eR8dd5ffOAcp-2260351

I extracted one of the read of this region of interest and align it again using ambig=toss and also ambig=all . Here are the results for ambig=toss.

M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    99  chr14   63006989    42  98M =   63007016    156 AATTTACGGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAG  GHAAEHFGGFCEFHHHHG3GFHGAE2GHHHBGFGHBGFHHHHHHHHFFGHDGGHH@DFHFBGHHGGEEGHGDFBGHHHHHGFGHBFGHEGCC/FC//@  NM:i:1  AM:i:42
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    147 chr14   63007016    44  129M    =   63006989    -156    CAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAGCCCGCATCGCCAAGTCAATCCTAAGCCAAAAGAACAAAGCTGGAGGCATCACACTACC   FHGCF11HHHHHD>GF0GG2BFHHHHHGDDFFGFFHGEGFHFFBHHGEBHGHFFFFHGGHGGEHHHHHHEE?CGE?ACGHHFHHGFFHHDHFCCGG?HFHGAF02HHFBABEAFHHHHHHFHGGA30HH   NM:i:0  AM:i:44

and here for ambig=all. You can see the results from ambig=toss are also there in addition to other region. Thus the read should be flagged as multimapped and not be reported in the ambig=toss mode.. no ?

M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    99  chr14   63006989    42  98M =   63007016    156 AATTTACGGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAG  GHAAEHFGGFCEFHHHHG3GFHGAE2GHHHBGFGHBGFHHHHHHHHFFGHDGGHH@DFHFBGHHGGEEGHGDFBGHHHHHGFGHBFGHEGCC/FC//@  NM:i:1  AM:i:42 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    147 chr14   63007016    44  129M    =   63006989    -156    CAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAGCCCGCATCGCCAAGTCAATCCTAAGCCAAAAGAACAAAGCTGGAGGCATCACACTACC   FHGCF11HHHHHD>GF0GG2BFHHHHHGDDFFGFFHGEGFHFFBHHGEBHGHFFFFHGGHGGEHHHHHHEE?CGE?ACGHHFHHGFFHHDHFCCGG?HFHGAF02HHFBABEAFHHHHHHFHGGA30HH   NM:i:0  AM:i:44 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    369 chr10   7101478 40  98M chr14   63007016    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 2:N:0:59    321 chr10   7101420 43  129M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    369 chr10   11774921    40  98M chr14   63007016    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 2:N:0:59    321 chr10   11774863    43  129M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    369 chr10   15959217    40  98M chr14   63007016    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 2:N:0:59    321 chr10   15959159    43  129M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 1:N:0:59    369 chr10   21042081    40  98M chr14   63007016    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:2109:9321:20334 2:N:0:59    321 chr10   21042023    43  129M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5

enter image description here

edit : check the comment for an additional example

bbmap
• 4,055 views • link
written by Nicolas Rosewick Nicolas Rosewick

Are those PCR duplicates (i.e. independent reads that are mapping in the same position)? If you used ambig=toss then one read that maps in several positions would not be included.

• 0 views • link
written by GenoMax GenoMax

Looking at the MAPQ and NM tag, the primary alignment is slightly better than the secondary alignments - read 1 has an edit distance of 1 and read 2 has an edit distance of 0 for the primary alignment, while read 1 has an edit distance of 2 and read 2 has an edit distance of 1 for the secondary alignment. That's more obvious with the "sam=1.4" cigar strings, but the fact that the pair's combined edit distance was 2 less for the primary than secondary alignments is why it was declared unambiguous.

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written by Brian Bushnell Brian Bushnell

I checked a little bit more in detail. Here's an alignment for a pair of reads in ambiguous=all

M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   99  chr14   63006989    42  98M =   63006989    125 AATTTACAGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGCAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAG  CEGBGHHH3A5ADAAF5BGHFHGGGHFGFFFFHG3FCCGHHHHGFHGHHGD@BF@@4F33F3ECGFGFC3?GGHHF4?FHBFFHGFDB/F/FCG@A/0  NM:i:1  AM:i:42 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   369 chr10   7101478 40  98M chr14   63006989    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   369 chr10   11774921    40  98M chr14   63006989    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   369 chr10   15959217    40  98M chr14   63006989    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   369 chr10   21042081    40  98M chr14   63006989    0   *   *   NM:i:2  AM:i:40 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   147 chr14   63006989    44  125M    =   63006989    -125    AATTTACAGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAGCCCGCATCGCCAAGTCAATCCTAAGCC   D1GBHFF<?11EHG<00C<?CEF2@2ACDB23DF2?3F3BFHHEHF4FF?GFHHEFFDGGEHDFB?4BGEBHHHEFHFHHHHHGDEHFE/G5G3F?0>CEGEAEAEFHDBBFEFEBDBDFCFFHH   NM:i:0  AM:i:44 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   321 chr10   7101451 43  125M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   321 chr10   11774894    43  125M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   321 chr10   15959190    43  125M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   321 chr10   21042054    43  125M    chr14   63006989    0   *   *   NM:i:1  AM:i:43 NH:i:5

So chr14:63006989 is the primary alignment as the AM score is the highest. To confirm I ran BBmap using ambiguous=toss and it gives me the right alignment :

M00991:78:000000000-AP8FW:1:1112:20035:11465 1:N:0:59   99  chr14   63006989    42  98M =   63006989    125 AATTTACAGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGCAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAG  CEGBGHHH3A5ADAAF5BGHFHGGGHFGFFFFHG3FCCGHHHHGFHGHHGD@BF@@4F33F3ECGFGFC3?GGHHF4?FHBFFHGFDB/F/FCG@A/0  NM:i:1  AM:i:42 NH:i:1
M00991:78:000000000-AP8FW:1:1112:20035:11465 2:N:0:59   147 chr14   63006989    44  125M    =   63006989    -125    AATTTACAGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAGCCCGC

However when I go to the location of the primary alignment (chr14:63006989) and copy the exact sequence where the reads align (chr14:63006989-63007113) : AATTTACAGATTCAATGCCATCCCCATCAAGCTACCAATGACTTTCTTCACAGAATTGGAAAAAACTACTTGAAAGTTCATATGGAACCAAAAAAGAGCCCGCATCGCCAAGTCAATCCTAAGCC

and align it on hg19 using blat I found two perfect locations :

  • chr14:63006989-63007113 : ok !
  • chr8:94422483-94422607 ??????

Here's the blat output : http://grch37.ensembl.org/Homo_sapiens/Tools/Blast/Results?db=core;tl=yRMn9fQ8AuuM68UD-2286190

The second alignment is not reported in the ambiguous=all mode ? But here this read is clearly a multimap one ..

Brian could you clarify this point ?

Thank you for your time

• 0 views • link
written by Nicolas Rosewick Nicolas Rosewick

For paired reads, the mapping score also takes into account the insert size; the score is higher the closer it is to the mean insert size. If you map those reads as single-ended rather than paired, they will all be considered ambiguous. Possibly, I should reduce the effect of insert size when determining whether a mapping is ambiguous.

• 0 views • link
written by Brian Bushnell Brian Bushnell

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