My fastq file is 6GB, I got the quals file is more than 12GB. Is it right?
From http://biostar.stackexchange.com/questions/1389/how-to-generate-a-consensus-fasta-sequence-from-sam-tools-pileup We use awk and perl to get fasta by
awk '/^@chr1$/,/^+$/' consensus.fastq | perl -pe "s/@/>/ ; s/\\+//" > chr1.fasta
The sample data
@chr1
nnnnnnnagatagaaataCACGATGCGAGCAATCAAATTTCATAACATCACCATGAGTTT
GGTCCGAAGCATGAGTGTTTACAATGTTTGAAtaCCTTATACAGTTCTTATACATACTTT
ATAAATTATTTCCCaagctgttttgatacactcactaacagaTATTCTATAGAAGGAAAA
+
!!!!!!!????????BBBEEEHKKKKKKKKKKKKNNNNNNQQNNNNNNQWWWW7WZWWWZ
ZZZ]]]`````````>]]]]]]]ZTQQQTQNNKKKKKKHKKHHHEEEEEEEHHHHHHHHH
HKKHHHHHHEEEEEBBBBBBBBBBBB?=B@BBBBBB??BBBBEEEEEEEEEEHKNNNNNQ
Now I want to extract the qual for each chromosome. But the qual score for each chromosome all beginning with "+", how can I extract them?
Thanks.
2 answers
Here is quick and extremely dirty python script to pull out fastq quality not making assumptions about line wrapping:
import sys
inFile = open(sys.argv[1],'r')
header = ''
qual = ''
seqs = False
quals = False
for line in inFile:
if line[0] == "@":
if header != '':
print ">" + header
print qual
header = line[1:].strip()
quals = False
qual = ''
elif line[0] == "+":
quals = True
else:
if quals:
qual += line.strip()
print ">" + header
print qual
Save as yourName.py and run it by: python yourName.py yourFile.fastq > output.quals
edit * There was a mistake in the code where the qual variable wasn't being reset.
edit **
Here is the script to get just one entry:
import sys
inFile = open(sys.argv[1],'r')
queryHeader = sys.argv[2]
header = ''
qual = ''
seqs = False
quals = False
for line in inFile:
if line[0] == "@":
if header != '':
if header == queryHeader:
print ">" + header
print qual
sys.exit()
header = line[1:].strip()
quals = False
qual = ''
elif line[0] == "+":
quals = True
else:
if quals:
qual += line.strip()
print ">" + header
print qual
Save it as yourName.py. Use it by: python yourName.py yourFile.fastq "entry name"
No, it is 37.8GB. Could you please double check your code?
Oops, there was a mistake. I've fixed it.
Now I got:There are many returns, is it correct?
chr2 !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! ]]]`
G]]`````cfTcffcfcOilifffEciiiififfcccccccfccffil Ullllliorrrrooiiooorueuuuuruxuuuxxrrrroorrrrrolllliilloooororoololoroollllllllllliilllrr QQQQQQQHQQQQQQQQQQQQQQQQTTTTQQQQQHQNNNNNNNNNNNNNKKKKKKKKHHKNNKKKNTTTTWWWQWZZZZT`]ccccifcllllilllooorrooooorlflllooooil
]]]WWWWWTTTTTTTQWZZ]Z]]```
]]Z]Z]]]]]]]]]cccfcliioouuuuuuu{xxuuuuuruxxxx{{xx{xuuurrorlllloooorrrrooooooooouorrloouuuu
updated: If I only want to get qual for chromosome 1, how to change code?
I've added the code to just get one entry.
I've added the scrip for getting just one entry. Make sure you typed the name of the entry correctly with quotes if there are spacing. If you didn't type it correctly, it will just give you the last entry.
Many many many thanks.
line[0] can be '+' for one of the qual lines if the phred33 score is 10. So maybe this code may break in some cases.
0 1 2 3 4 01234567890123456789012345678901234567890 !"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHI
fq2fa tool extracts qual scores from fastq file.
Here is the link : http://www.phyloware.com/Phyloware/XSTK.html
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It quality doesn't wrap lines can't you just grep for "+"?