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Sequence Number Count In Fastq.Gz File
10
Entering edit mode
6.5 years ago
Bioscientist ♦ 1.7k

Do we have any easy, fast way to know how many sequences contained in paired-end fastq.gz file? One simple way I think to calculate is to count the # of lines in fastq file divided by 4. (Four line for one sequence)

But I'm afraid it'll be quite slow for the calculation due to the large size of fastq.gz

What about the sequences in .sai/.sam file? (Because I want to guarantee the quality by comparing sequences in fastq file, and how many sequences been processed in .sai/.sam file)

The only way I can think of, is that we have the error report of .sai/.sam file generation, in which we get the information like "10000000 sequences have been processed". I can print this line by python, but how can I print out this number out of the line?

thx

To Ale: thx, but what's the rationale for your first command? I mean about ^@ Just look at the fastq.gz file below, where is ^@ ? I see many @, but not ^

@IL11_266:1:67:0:838/1
AAAAAAAAAAAAAAAAAAAAANNANNNANANAAAAA
+
@@AAAAAAA@AAAAAABAAAB&&B&%%B%>%=<>>>
@IL11_266:1:67:3:594/1
AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAC
+
@@AAAAAAA@AAA?AA@A@AB?AB@AAB7>&=><A2


Edit again: Also I try both of the commands, and find the result is 2-fold difference. I compared with .sai file error report, which said 853813 sequences have been processed, then should say 'zgrep' command double counts.

[x@hpcc01 bwa2]$zcat ERR002356_1.recal.fastq.gz | echo$((wc -l/4))
853813
[x@hpcc01 bwa2]$zgrep -c '^@' ERR002356_1.recal.fastq.gz 1643596  EDIT: THX. But I'm not dealing with one file. Plz look at below: #!/usr/bin/python import os,sys,re import gzip import commands path = "/home/xug/nearline" for file in os.listdir(path): if re.match('.*\.recal.fastq.gz', file): fullpath = os.path.join(path, file) result = commands.getoutput('zcat fullpath |wc -l') numseqs = int(result)/4.0 print numseqs  Problem is, I define 'fullpath' here for all fastq files, but after being put under ' ', seems this fullpath doesn't work...How can I solve this problem? thx Problem solves....fullpath is variable. ..so 'zcat '+fullpath+' |wc -l' ADD COMMENTlink 2 Entering edit mode @bioscientist, this is a very good point - [z]grep cannot be used (like for fasta) because @ and + can also occur in the quality line. ADD REPLYlink 1 Entering edit mode ^ means --> begins with ... ADD REPLYlink 1 Entering edit mode The following should do the trick: zgrep -c '^@.*/[0-9]$' fastq.gz

1
Entering edit mode

In general, checking for a terminal digit will not work because Sanger-encoded Fastq qualities include characters in the range ASCII 33 to 126, that is to say the qualities may contain digits. Your regex will still potentially match quality lines.

17
Entering edit mode
19 months ago
United States

Your method should also work and it should be pretty fast:

zcat my.fastq.gz | echo $((wc -l/4))  For SAM it's: cat my.sam | grep -v '^ *@' | wc -l  I'm not sure how to interact with .sai files. NOTE1: You can call the above Bash commands from Python: import commands result = commands.getoutput('zcat my.fastq.gz | wc -l') numseqs = int(result) / 4.0  If you are doing Bioinfromatics you want to have the GNU toolset which includes the Bash shell (it's default on Linux and Mac, on Win you can install Cygwin) NOTE2: I'm assuming that all input files have a newline at the end. It's easy to check: run zcat my.fastq.gz | tail -n 1 | cat -E  if you see a dollar sign ($) then everything is OK. Conversely, you may have generated the files on Windows or from a newbie/ignorant code that does not place a newline at the end of the file, then you will not see a the dollar sign. In that case sanitize the files like this:

zcat my.fastq.gz  | ruby -pne '$_.chomp!;$_ << "\n"' | gzip > good.fastq.gz


NOTE3: I'm assuming that your FASTQ files don't wrap lines. One line per read. You can test like this:

zcat my.fastq.gz  | ruby -e '
skip_line = false
last_char = "+"

while gets
if skip_line
skip_line = false
next
end

if $_ =~ /^@/ and last_char == "+" last_char = "@" elsif$_ =~ /^\+/ and last_char == "@"
last_char = "+"

else
STDERR.puts "WARNING: fastq lines wrap at line #{.}" exit(1) end skip_line = true end STDERR.puts "fastq lines do not wrap" '  NOTE4: Instead of all of the above you can use a filesystem with online compression (i.e. ZFS) and do all the analysis on fastq files instead of fastq.gz ADD COMMENTlink 2 Entering edit mode Uh, you are making the assumption that the Fastq file isn't wrapping the sequences. Although this is uncommon, it's allowed within the standard. Also, SAM files may have a separate header section, you need to make sure only to count the aligned reads. ADD REPLYlink 0 Entering edit mode thx Ale, but this is shell command, right? I want to do this within Python script. ADD REPLYlink 0 Entering edit mode yeah the line counting thing to easily flummoxed by missing end-of-file carriage returns (bad but common) and the SAM thing is just outright wrong in headered SAM files. ADD REPLYlink 0 Entering edit mode @Jeremy, @Ketil - I took into account your comments. ADD REPLYlink 4 Entering edit mode 18 months ago summerela • 90 United States I'm a bit late to the party, but here's an answer using gnu parallel that should do the trick.. and quickly: parallel "echo {} && gunzip -c {} | wc -l | awk '{d=\1; print d/4;}'" ::: *.gz


This assumes your fastq files are gzipped and in standard fastq format.

1
Entering edit mode

tks summerela \o/

1
Entering edit mode
16 months ago
Cambridge, MA

Here's a method to count the number of reads from the BAM index file:

https://gist.github.com/mdshw5/73c6591237c7a9f88518

The speed of this method is independent of the number of reads in your BAM file.

0
Entering edit mode
19 months ago
Seattle, WA USA

I posted a solution here that uses GNU Parallel: https://www.biostars.org/p/63816/#67136