How to convert output from bowtie1 to Genomic ranges

Hello, I have output from bowtie 1

bowtie  '~/UCSC/hg38/Sequence/BowtieIndex/genome'  -f '~/sample.fa'  
 -v 1  -k 1 -p 6 --al outputAligned --un outputNotAligned > randomtest1

that it looks like that:

    fread("randomtest1")

     V1      V2 V3    V4        V5                                     V6                                     V7 V8 V9
     1: t00000001 1148630  +  chrX  69672575               GGAATACCGGGTGCTGTAGGCTTT               IIIIIIIIIIIIIIIIIIIIIIII  1 NA
     2: t00000002 1078059  - chr11  64891202                  GGCTGTCAATTCATAGGTCAG                  IIIIIIIIIIIIIIIIIIIII  0 NA
     3: t00000003 1038720  + chr19  53787930                AAAGTGCTGCGACATTTGAGCGT                IIIIIIIIIIIIIIIIIIIIIII  0 NA
     4: t00000004 1027976  + chr13  91351360                 TATTGCACTTGTCCCGGCCTGT                 IIIIIIIIIIIIIIIIIIIIII  0 NA
     5: t00000005  948116  - chr17   1713913                 ACAGTTCTTCAACTGGCAGCTT                 IIIIIIIIIIIIIIIIIIIIII  0 NA
    ---                                                                                                                         
611991: t01137877       1  +  chr6  21215555                   TCCTTTCAGCTCTACAACTC                   IIIIIIIIIIIIIIIIIIII  0 NA
611992: t01137878       1  + chr12 110012992       ATCCTGGTAAGGTTGGACTGCAGCCCTTTTCT       IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  0 NA
611993: t01137880       1  +  chrM     11393 TCCACTTATGACTCCCTAAAGCCCATGTCGAAGCCCCC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  0 NA
611994: t01137885       1  +  chr7 133383687      TGTCGACTTTGATATTTTGGTTACCTGAGGATT      IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  0 NA
611995: t01137887       1  - chr20  62414571      AGCCGAATGACCATGGCTGTGTGGAGCCGTGAC      IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII  0 NA

so the file is not a sam / bam or bed.

I believe that V5 has the "1-based offset into the forward reference strand where leftmost character of the alignment occurs" as described in [Bowtie Manual].[1] I checked the 1st read manually in Genome Browser, and it starts in chrX 69,672,576. So I can calculate the length of each sequence and add it to the V5 column +1, for the +strand. But I am not sure how to calculate the regions of the - strand.

I want to convert it to a Grange object

Thank you in advance

rna-seq genomicranges bowtie

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updated 7.5 years ago by ATpoint

• written 7.5 years ago by Konstantinos Yeles

1 answer

The simplest solution would be to make bowtie print output in sam format (option --sam), saving the output in BAM format, followed by reading the data into R with the GenomicAlignments package (readGAlignments function) which can then be converted to GRanges with granges(). Please check the documentation of the package.

bowtie --sam (your options...) | samtools view -o out.bam

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written 7.5 years ago by ATpoint

I would have done that but that output is a part of a workflow of a tool I use.

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written 7.5 years ago by Konstantinos Yeles

Ok I see. There is a script bowtie2sam.pl in the legacy folder of samtools that you could use to convert the bowtie output to SAM/BAM, followed by readGAlignments.

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written 7.5 years ago by ATpoint

I tried the bowtie2sam.pl and got :

    Argument "IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII" isn't numeric in numeric eq (==) at ~/bowtie2sam.pl line 70, <> line 861046.
Argument "chr1" isn't numeric in addition (+) at ~/bowtie2sam.pl line 67, <> line 861047.

and then with samtools:

[E::sam_parse1] missing SAM header
[W::sam_read1] Parse error at line 1
[main_samview] truncated file.

and finally with readGAlignments

readGAlignments("randometest.sam")
[bam_header_read] EOF marker is absent. The input is probably truncated. [bam_header_read] invalid BAM binary header (this is not a BAM file). Error in value[[3L]](cond) :   failed to open BamFile: SAM/BAM header missing or empty   file: 'randometest.sam'

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written 7.5 years ago by Konstantinos Yeles