strange Illumina txt format

[HESmith]

BFAST contains a Perl script (ill2fastq) for this conversion.

[Kaas]

Thanks mastal
I arrived at this thread from http://seqanswers.com/forums/showthread.php?t=5210 because i needed to convert from Illumina 1.5 (phred64) to Illumina 1.9 (Phred33). i misread and used the perl script from this this thread.

[mastal]

Hi Kaas,

What are you trying to achieve by using this script?
Because your starting file, SRR823966_2.fastq, looks like it's already in fastq format.

The script converts Illumina's old qseq.txt format to fastq.
Since your file is not in qseq format, the script is not extracting the right information into the variables,
which is why you are getting all those 'Use of uninitialized value' errors.

[Kaas]

I saved the above mentioned script as Sanger.pl and tested it on the first 12 lines of a Illumina 1.5 fastq file

perl Sanger.pl SRR329951_2.fastq.fa > newfile.fq

put I am given the following errors for all lines
Use of uninitialized value in transliteration (tr///) at Sanger.pl line 23, <> line 1.
Use of uninitialized value in transliteration (tr///) at Sanger.pl line 29, <> line 1.
Use of uninitialized value $run_id in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $lane in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $tile in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $x in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $y in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $read in concatenation (.) or string at Sanger.pl line 39, <> line 1.
Use of uninitialized value $bases in concatenation (.) or string at Sanger.pl line 43, <> line 1.
Use of uninitialized value $q_line in concatenation (.) or string at Sanger.pl line 43, <> line 1.

Any idea what I am doing wrong?

cat SRR823966_2.fastq
@SRR823966.19590458 FCC076MACXX:3:2308:13081:200822 length=90/2
GGAGACTGTAGTTGGGTAGAGGGTCAGGTGTCGGGGTACTCGTGAGTTGTGTTGGCGGTTGTGTAGTTTAGTATATGTGTGATTGTTTGT
+SRR823966.19590458 FCC076MACXX:3:2308:13081:200822 length=90
BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB
@SRR823966.19590459 FCC076MACXX:3:2308:14378:200834 length=90/2
AAACATGTAACTTATTTATTTTTACCATTGTTGGGCTGGCGTGGTGGTTTGTGAGTGGGCCTTTGAGTTTGATGTCAGTCTGGTCTGTGT
+SRR823966.19590459 FCC076MACXX:3:2308:14378:200834 length=90
PPJSSS\aQQKR]JQbfQ]biiiJJRJR[RSbfhiHYbgHHO^eaeheGW[bfHW]bgBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB

head -12 newfile.fq
@@SRR823966.19590458 FCC076MACXX:3:2308:13081:200822 length=90/2_::::/

+

@GGAGACTGTAGTTGGGTAGAGGGTCAGGTGTCGGGGTACTCGTGAGTTGTGTTGGCGGTTGTGTAGTTTAGTATATGTGTGATTGTTTGT_::::/

+

@+SRR823966.19590458 FCC076MACXX:3:2308:13081:200822 length=90_::::/

+

@BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB_::::/

+

@@SRR823966.19590459 FCC076MACXX:3:2308:14378:200834 length=90/2_::::/

+

@AAACATGTAACTTATTTATTTTTACCATTGTTGGGCTGGCGTGGTGGTTTGTGAGTGGGCCTTTGAGTTTGATGTCAGTCTGGTCTGTGT_::::/

+

@+SRR823966.19590459 FCC076MACXX:3:2308:14378:200834 length=90_::::/

+

@PPJSSS\aQQKR]JQbfQ]biiiJJRJR[RSbfhiHYbgHHO^eaeheGW[bfHW]bgBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB_::::/

+

@@SRR823966.19590460 FCC076MACXX:3:2308:15143:200791 length=90/2_::::/

+

@CTCGAGCAGGAGAGGGGCCCTGGCTGCTGAGGGGTCCCTGTCCAATAACCCCCACACCGATCATGTCCCTCACAGTTTCCATCTCAGACG_::::/

+

@+SRR823966.19590460 FCC076MACXX:3:2308:15143:200791 length=90_::::/

+

@BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB_::::/

+

[sklages]

Do you know how to run the perl script in unix and make it utilize the fastq file? thanks.

to run: perl myScript.pl FASTQ_file > newfile.fq

It is not intended to work with fastq files but with qseq files.

[jamminbeh]

Do you know how to run the perl script in unix and make it utilize the fastq file? thanks.

[epigen]

convert Illumina scores into Phred scores in a BAM file

Assuming that this is a .qseq.txt file, you can convert it to fastq format with the following perl script (note that this script converts the quality values to phred+33 format):

Although this thread is quite old, I found it extremely useful. Thanks for providing the efficient way to convert Illumina scores into Phred scores, rmdavies!
I used it to transform the scores in a BAM file:

samtools view -h Illumina_score.bam | perl -lane '$"="\t"; if (/^@/) {print;} else {$F[10]=~ tr/\x40-\xff\x00-\x3f/\x21-\xe0\x21/;print "@F"}' | samtools view -Sbh - > Phred_score.bam

Saved us a lot of fastq file transformations and we did not have to run all the BWA alignments again.

[Asifullah]

Thank you very much rmdavies! You are right and my file is a .qseq one! By converting the file, now I can get the alignment with bwa. I'm a beginner with illumina data, and I could not know what is this format.
thanks again for the precious help!!!
M.Elena

I am a new user of illumina data and i myself facing the same type of read format which u have pointed. I want to convert it in to simple FASTq format. could you please give the commend line for running this perl script. I can,t find its running commend line for successful operation. My email address is ([email protected]). i will highly oblige to lessen from your side.
regard,
asifullah

[m_elena_bioinfo]

Thank you very much rmdavies! You are right and my file is a .qseq one! By converting the file, now I can get the alignment with bwa. I'm a beginner with illumina data, and I could not know what is this format.
thanks again for the precious help!!!
M.Elena

[rmdavies]

This looks like an Illumina .qseq.txt file, although I'm a bit puzzled as to why the last base of the sequence is in its own column. Possibly this is an artifact from when you copied the data into the forum?

Assuming that this is a .qseq.txt file, you can convert it to fastq format with the following perl script (note that this script converts the quality values to phred+33 format):

#!/usr/bin/perl

use strict;
use warnings;

while (<>) {
    chomp;
    my ($instr, $run_id, $lane, $tile, $x, $y, $index, $read,
	$bases, $q_line, $filter) = split /\t/, $_;

    # Turn dots into Ns in the base calls
    $bases =~ tr/./N/;

    # Convert Illumina's quality values to true Phred scale
    $q_line =~ tr/\x40-\xff\x00-\x3f/\x21-\xe0\x21/;

    if ($index) {
	print "\@${instr}_$run_id:$lane:$tile:$x:$y\#$index/$read\n";
    } else {
	print "\@${instr}_$run_id:$lane:$tile:$x:$y/$read\n";
    }
    print "$bases\n+\n$q_line\n";
}

Once you have your fastq file, you should be able to use it as input to bwa in order to get your alignment.

[m_elena_bioinfo]

Here is another example of my txt file:

HWUSI-EAS68R 1 3 1 1097 20058 0 1 AGACCTCATTATTATCTGTGTGTCTGCATTTTCTAATCCTTTTTGCCCCAG ]^aaa]][]]E^^^`]]]^]aaaaaaa_a
\aa_``_a_aa[a]]`YZ[WSY 1
HWUSI-EAS68R 1 3 1 1097 17901 0 1 TGCTGATGAGATTTATGACTGCAAGGTGGAGCACTGGGGCCTGGACCAGCC bbbbb]^`Y`Kbbbbaaa_`^^b^b]\]_
`bbbbbbb^b_b^bbb_b\bbb 1
HWUSI-EAS68R 1 3 1 1097 17710 0 1 TGGCGCACCCTAAGGCTCAGTCAGTAACCCGTACACAAACTCGTCCCTGCA BBBBBBBBBBBBBBBBBBBBBBBBBBBBB
BBBBBBBBBBBBBBBBBBBBBB 0

[m_elena_bioinfo]

Dear NGS-users,
I have a problem for the analysis of reads from f single-read 36bp SureSelect run (Illumina).

My reads file is in .txt format.

I usually use BWA for the alignment and then use SAMTOOLS for the pileup.
With alignment step, BWA returns me a 64kb sai file, and a sam file of 27Kb of dimension. Probably these files are uncorrect and incomplete. The next step to convert sam2bam crushes with this message:

[samopen] SAM header is present: 657 sequences.
[sam_read1] reference 'SN:hg18_knownGene_uc002qho.2 LN:16765

' is recognized as '*'.
[main_samview] truncated file.


I think that the problem is the strange format of the initial txt file (here is an example):
HWUSI-EAS68R 1 3 1 995 11343 0 1 .CTTG........T.....GGGG............................ BBBBBBBBBBBBBBBBBBBBBBBBBBBBB
BBBBBBBBBBBBBBBBBBBBBB 0
HWUSI-EAS68R 1 3 1 995 18576 0 1 .ACAG........C.....GTTG............................ BBBBBBBBBBBBBBBBBBBBBBBBBBBBB
BBBBBBBBBBBBBBBBBBBBBB 0

Why is so strange my txt file?
May depend on what?
Thank you very much
M.Elena