Entering edit mode
6.2 years ago
manojkumarbioinfo
▴
100
Hai,
I have a fastq file generated by Hiseq machine. i wish to extract the bar code of the sequence from the fastq files.
It's probably in the header and there's likely no reason to do so. It'd help if you provided a bit more detail.
I'm posting my Header file of my fastq.
I'm running Qimme 2 for running cansava 1.8 the file name should be in the particular format for example L2S357_15_L001_R1_001.fastq.gz. The underscore-separated fields in this file name are the sample identifier, the barcode sequence or a barcode identifier, the lane number, the read number, and the set number.
I wrongly renamed the original file so i cant able to run my command.
In this example you appear to have lost the index sequence. It should be present in
1:N:0:4
in place where4
is. I should look like1:Y:18:ATCACG
.you have sample number (4) in place of index. By any chance, is this from base space v2? Refer to sample sheet from sequencing core for sample 4. manojkumarbioinfo.