Hi all,
I used poretools to extract fastq sequences from fast5 PASS files with no problem. However, I was unable to extract valid sequences from files archived on the SKIP folder. i.e
$ poretools stats pass_read.fast5
total reads 1
total base pairs 1864
mean 1864.00
median 1864
min 1864
max 1864
N25 1864
N50 1864
N75 1864
$ poretools stats skip_read.fast5
WARNING:poretools:No valid sequences observed.
I have plenty of files in the skip folder (I suspect due to computer resources) and I would like to obtain as much information as possible from the sequencing process.
Attached you will find both files.
Any advice will be appreciated
pass_read.zipskip_read.zip
Hi all, I used poretools to extract fastq sequences from fast5 PASS files with no problem. However, I was unable to extract valid sequences from files archived on the SKIP folder. i.e
I have plenty of files in the skip folder (I suspect due to computer resources) and I would like to obtain as much information as possible from the sequencing process. Attached you will find both files. Any advice will be appreciated pass_read.zip skip_read.zip