.SAM to .BAM with SAM file header @PG

[Richard Finney]

Hmmmm.

You might be messing up with the sed command:

sed s/.fa//

that's saying change "anychar+f+a" to nothing.

"f" and "a" appear to be legitimate GERALD (or whatever, "export") quality value, so they'll get unintentionally changed to null , as well as the intended strings likes "chr1.fa" --> "chr1"

Glance at the input file for legitimate quality values (the field after the sequence field)

In sed language , putting a backslash before dot (i.e. \. ) means "period" to distinguish from the sole dot (i.e. .) which means "any character".

[SDBP]

On another line I see :

ABC-DE2 1 4 1 3 1978 0 1 CAATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN _]_BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB QC

This way I will have to go through the whole file?

[SDBP]

Sorry, the above was from the file where I did not remove the .fa

Below is from the file which I am working on:

ABC-DE2 1 4 1 3 1347 0 1 TTTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN_BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB QC

[SDBP]

Line 284:

ABC-DE2 1 4 1 3 119 0 1 GAGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB QC N


Line 285:
ABC-DE2 1 4 1 3 1347 0 1 TTTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN fa_BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB QC N


I see that there is the extra 'fa' in line 285.....
can I try deleting it?
will deleting it work?

[Richard Finney]

The perl code is ...

if(scalar(@t) < EXPORT_SIZE) {
my $msg="\nERROR: Unexpected number of fields in export record on line $line_no of read$read_no export file. Found " . scalar(@t) . " fields but expected " . EXPORT_SIZE . ".\n";
$msg.="\t...erroneous export record:\n" . $line . "\n\n";
die($msg);

EXPORT_SIZE is 22 ( EXPORT_SIZE => 22 )

It's complaining that line 285 has only 21 fields.

What are on lines 284 and 285 ?

[SDBP]

samtools-0.1.16

[Richard Finney]

What version of samtools?

[SDBP]

perl export2sam.pl --read1=my_export.txt > my_export.sam

[Richard Finney]

What is the full command you are using for export2sam.pl ?
Beware that the input is supposed to be a "GERALD" type of file (also know as "illumina export file").

[SDBP]

I am dealing with the same kind of SAM files - header @PG.
I tried -S option, it didn't work.
First I saw the segmentation fault. When I fixed that and ran

samtools view -bt my.fa.fai my.sam > my.bam - It showed the following

[sam_read1] reference 'chr3.fa' is recognized as '*'.
[sam_read1] reference 'chr1.fa' is recognized as '*'.
[sam_read1] reference 'chr19.fa' is recognized as '*'.
[sam_read1] reference 'chr3.fa' is recognized as '*'.

Then I did a sed s/.fa// on the input file before doing export2sam.pl and ran export2sam.pl, it throws the following errors:

ERROR: Unexpected number of fields in export record on line 285 of read1 export file. Found 21 fields but expected 22.
...erroneous export record:
ABC-GA2 1 4 1 3 1347 0 1 TTTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN_BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB QC

Any insight will be helpful.
Any other SAM to BAM tools known for sam files with @PG ?????

[kmcarr]

Hi Richard,

I do want to convert SAM to BAM, it output error when I used "samtools view -b in.sam -o out.bam". I checked the header of SAM file, it comes with @PG. I don't know how to deal with it?

Thanks

Emily,

As Richard said you need to us the -S option (in addition to your other options) to tell samtools view that the INPUT is in SAM format. By default samtools view expects a BAM file as input but you are giving it a SAM file, that's what is causing an error.

[emilyjia2000]

Hi Richard,

I do want to convert SAM to BAM, it output error when I used "samtools view -b in.sam -o out.bam". I checked the header of SAM file, it comes with @PG. I don't know how to deal with it?

Thanks

[Richard Finney]

use -S parameter

Usage: samtools view [options] <in.bam>|<in.sam> [region1 [...]]

Options: -b output BAM
-h print header for the SAM output
-H print header only (no alignments)
-S input is SAM
-u uncompressed BAM output (force -b)
-1 fast compression (force -b)
-x output FLAG in HEX (samtools-C specific)
-X output FLAG in string (samtools-C specific)
-c print only the count of matching records
-L FILE output alignments overlapping the input BED FILE [null]
-t FILE list of reference names and lengths (force -S) [null]
-T FILE reference sequence file (force -S) [null]
-o FILE output file name [stdout]
-R FILE list of read groups to be outputted [null]
-f INT required flag, 0 for unset [0]
-F INT filtering flag, 0 for unset [0]
-q INT minimum mapping quality [0]
-l STR only output reads in library STR [null]
-r STR only output reads in read group STR [null]
-? longer help

[emilyjia2000]

Hi
I used export2sam.pl to convert export.txt to .sam. I checked the newly generated SAM file with header @PG. When I tried to use command line, like
" samtools view -b in.sam -o out.bam "
to generate BAM file, it occurs errors:

[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).
[main_samview] fail to read the header from "in.sam".

Does anybody know what's wrong with it? What command line I should use for converting SAM to BAM

Thanks