[Bioc-sig-seq] Rsamtools readPileup with Mosaik alignments

James MacDonald jmacdon at med.umich.edu
Wed Apr 21 17:34:06 CEST 2010


Hi,

I have found what I think is an infelicity with readPileup() when the 
alignment is done with software other than say BWA or Bowtie.

I am aligning SOLiD data, so my choices are rather limited. In order to 
do gapped alignments, I used Mosaik to do the alignment and then 
converted to bam files and proceeded from there using samtools.

When I use the readPileup() function, if I choose variant="SNP", it 
appears I am not reading in all the SNPs, and if I choose 
variant="indel", it appears I am reading in SNPs as well as indels.

I think this arises because of an expectation for the pileup format that 
is outlined on this page:

http://samtools.sourceforge.net/cns0.shtml 

where an indel should look like this, in the pileup output:

seq2  156 A  A  10  0  99  11  .$......+2AG.+2AG.+2AGGG <975;:<<<<<
seq2  156 *  +AG/+AG  71  252  99  11  +AG  *  3  8  0

In this case, both lines indicate an indel at the same position, so 
readPileup() with variant="SNP" will search for lines containing "*" in 
the third column, and remove a given line and the line preceding it. So 
in this case, both of these lines would be removed, as expected.

If variant="indel", then data from both lines are used, which is OK for 
the data above, but not so much for me.

This is because the output from pileup that I get when using the Mosaik 
aligned data doesn't follow that convention. Instead it looks like this:

chr10 50620982 G A 45 72 31 16 AAAAaaaaAaaaAAac  =<><@=9>@'7:@@:&
chr10 50623836 G A 60 63 30 19 AA.CAAAAAAAAAaAAAAA <9/::@<@A?:A@>4=:AB
chr10 50650827 * */-cca 162 162 22 26 * -cca 24 2 0 0 0
chr10 50650919 * +A/* 182 182 20 27 +A * 5 20 2 0 0
chr10 50651118 * */-t 72 72 29 51 * -t 48 3 0 0 0
chr10 50651155 * */-t 145 145 19 21 * -t 13 4 4 0 0
chr10 50651269 C Y 46 53 42 16 ,tT,,,,TtttTt,,, @A9;<<7<@>8>;0,,

So when I read these data using readPileup(<thefile>, variant="SNP"), I 
lose the SNP in the second line. If I read in indels using 
variant="indel", then the SNP in the second line will be read in.

I don't know if there are also instances where an indel takes two lines 
as in the samtools example above, but that would be the minority if so.

Best,

Jim



-- 
James W. MacDonald, M.S.
Biostatistician
Douglas Lab
University of Michigan
Department of Human Genetics
5912 Buhl
1241 E. Catherine St.
Ann Arbor MI 48109-5618
734-615-7826


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