Open fhu2008-tio opened 6 years ago
Only success once after install the soft, (step1 to step4 are all ok!)
but when repeat again ,fail at step 3 with no results file generated,
command: extract_sequences ecoli_filtered.fastq.corrected.fasta corrected_ecoli_25x.fasta 4800000 25)
no corrected_ecoli_25x.fasta.fasta.qual , no corrected_ecoli_25x.fasta.fasta.qv no corrected_ecoli_25x.fasta.fasta.frg no corrected_ecoli_25x.fasta.fasta
also, there were no errors, no warnings,as show below?
does anyone else can fix it ?
[root@localhost Genome_Assembly]# extract_sequences ecoli_filtered.fastq.corrected.fasta corrected_ecoli_25x.fasta 4800000 25
step 1: convert fasta to fastq step 2: convert fastq to CA step 3
Starting file 'ecoli_filtered.fastq.corrected.fasta.fastq.libname.frg'.
Processing SINGLE-ENDED SANGER QV encoding reads from: '/home/workplace/Genome_Assembly/ecoli_filtered.fastq.corrected.fasta.fastq'
GKP finished with no alerts or errors.
step 4 Longest picked cutoff: 12691 Scanning store to find libraries used. Added 0 reads to maintain mate relationships. Dumping 0 fragments from unknown library (version 1 has these) Dumping 7639 fragments from library IID 1 step 5 Longest picked cutoff: 12691 Scanning store to find libraries used and reads to dump. Added 0 reads to maintain mate relationships. Dumping 0 fragments from unknown library (version 1 has these) Dumping 7639 fragments from library IID 1
@fhu2008-tio This is the problem with the name of the file suffix, we have fixed this problem in the updated mecat. Thanks for using mecat!
Only success once after install the soft, (step1 to step4 are all ok!)
but when repeat again ,fail at step 3 with no results file generated,
command: extract_sequences ecoli_filtered.fastq.corrected.fasta corrected_ecoli_25x.fasta 4800000 25)
no corrected_ecoli_25x.fasta.fasta.qual , no corrected_ecoli_25x.fasta.fasta.qv no corrected_ecoli_25x.fasta.fasta.frg no corrected_ecoli_25x.fasta.fasta
also, there were no errors, no warnings,as show below?
does anyone else can fix it ?
[root@localhost Genome_Assembly]# extract_sequences ecoli_filtered.fastq.corrected.fasta corrected_ecoli_25x.fasta 4800000 25
step 1: convert fasta to fastq step 2: convert fastq to CA step 3
Starting file 'ecoli_filtered.fastq.corrected.fasta.fastq.libname.frg'.
Processing SINGLE-ENDED SANGER QV encoding reads from: '/home/workplace/Genome_Assembly/ecoli_filtered.fastq.corrected.fasta.fastq'
GKP finished with no alerts or errors.
step 4 Longest picked cutoff: 12691 Scanning store to find libraries used. Added 0 reads to maintain mate relationships. Dumping 0 fragments from unknown library (version 1 has these) Dumping 7639 fragments from library IID 1 step 5 Longest picked cutoff: 12691 Scanning store to find libraries used and reads to dump. Added 0 reads to maintain mate relationships. Dumping 0 fragments from unknown library (version 1 has these) Dumping 7639 fragments from library IID 1