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[ INFO] 2019-03-13 17:59:09 : Loading assembly: assembled.transcripts1.fasta
[ INFO] 2019-03-13 18:04:31 : Analysing assembly: assembled.transcripts1.fasta
[ INFO] 2019-03-13 18:04:31 : Results will be saved in transrate_results/assembled.transcripts1
[ INFO] 2019-03-13 18:04:31 : Calculating contig metrics...
[ INFO] 2019-03-13 18:21:02 : Contig metrics:
[ INFO] 2019-03-13 18:21:02 : -----------------------------------
[ INFO] 2019-03-13 18:21:02 : n seqs 808362
[ INFO] 2019-03-13 18:21:02 : smallest 100
[ INFO] 2019-03-13 18:21:02 : largest 10337
[ INFO] 2019-03-13 18:21:02 : n bases 212338608
[ INFO] 2019-03-13 18:21:02 : mean len 183.12
[ INFO] 2019-03-13 18:21:02 : n under 200 451171
[ INFO] 2019-03-13 18:21:02 : n over 1k 16170
[ INFO] 2019-03-13 18:21:02 : n over 10k 1
[ INFO] 2019-03-13 18:21:02 : n with orf 20778
[ INFO] 2019-03-13 18:21:02 : mean orf percent 52.74
[ INFO] 2019-03-13 18:21:02 : n90 247
[ INFO] 2019-03-13 18:21:02 : n70 381
[ INFO] 2019-03-13 18:21:02 : n50 689
[ INFO] 2019-03-13 18:21:02 : n30 10337
[ INFO] 2019-03-13 18:21:02 : n10 10337
[ INFO] 2019-03-13 18:21:02 : gc 0.43
[ INFO] 2019-03-13 18:21:02 : bases n 0
[ INFO] 2019-03-13 18:21:02 : proportion n 0.0
[ INFO] 2019-03-13 18:21:02 : Contig metrics done in 991 seconds
[ INFO] 2019-03-13 18:21:02 : Calculating read diagnostics...
[ERROR] 2019-03-13 18:21:36 : Snap found unmatched read IDs in input fastq files
[ERROR] Left files contained read id
'A00155:73:HC5FYDSXX:2:1101:9209:1000' and right files contained read id
'A00155:73:HC5FYDSXX:2:1102:20121:5368'. at the same position in the file
I read in some issue that it could be happening because of the read number /1 or /2. Despite the modification, it keeps not working so it is not the heading. I don't know how can I understand the error printed and therefore how to solve it.
Can someone help me? thanks a lot
The text was updated successfully, but these errors were encountered:
Hello, I am trying to use TransRate
Path/transrate-1.0.3-linux-x86_64/transrate --assembly=assembled.transcripts1.fasta,assembled.transcripts2.fasta,assembled.transcripts3.fasta left=RNAseq1.trimmed.fastq,RNAseq1.unpaired.fastq --right=RNAseq2.trimmed.fastq,RNAseq2.unpaired.sed.fastq
[ INFO] 2019-03-13 17:59:09 : Loading assembly: assembled.transcripts1.fasta
[ INFO] 2019-03-13 18:04:31 : Analysing assembly: assembled.transcripts1.fasta
[ INFO] 2019-03-13 18:04:31 : Results will be saved in transrate_results/assembled.transcripts1
[ INFO] 2019-03-13 18:04:31 : Calculating contig metrics...
[ INFO] 2019-03-13 18:21:02 : Contig metrics:
[ INFO] 2019-03-13 18:21:02 : -----------------------------------
[ INFO] 2019-03-13 18:21:02 : n seqs 808362
[ INFO] 2019-03-13 18:21:02 : smallest 100
[ INFO] 2019-03-13 18:21:02 : largest 10337
[ INFO] 2019-03-13 18:21:02 : n bases 212338608
[ INFO] 2019-03-13 18:21:02 : mean len 183.12
[ INFO] 2019-03-13 18:21:02 : n under 200 451171
[ INFO] 2019-03-13 18:21:02 : n over 1k 16170
[ INFO] 2019-03-13 18:21:02 : n over 10k 1
[ INFO] 2019-03-13 18:21:02 : n with orf 20778
[ INFO] 2019-03-13 18:21:02 : mean orf percent 52.74
[ INFO] 2019-03-13 18:21:02 : n90 247
[ INFO] 2019-03-13 18:21:02 : n70 381
[ INFO] 2019-03-13 18:21:02 : n50 689
[ INFO] 2019-03-13 18:21:02 : n30 10337
[ INFO] 2019-03-13 18:21:02 : n10 10337
[ INFO] 2019-03-13 18:21:02 : gc 0.43
[ INFO] 2019-03-13 18:21:02 : bases n 0
[ INFO] 2019-03-13 18:21:02 : proportion n 0.0
[ INFO] 2019-03-13 18:21:02 : Contig metrics done in 991 seconds
[ INFO] 2019-03-13 18:21:02 : Calculating read diagnostics...
[ERROR] 2019-03-13 18:21:36 : Snap found unmatched read IDs in input fastq files
[ERROR]
Left files contained read id
'A00155:73:HC5FYDSXX:2:1101:9209:1000'
and right files contained read id
'A00155:73:HC5FYDSXX:2:1102:20121:5368'.
at the same position in the file
I read in some issue that it could be happening because of the read number /1 or /2. Despite the modification, it keeps not working so it is not the heading. I don't know how can I understand the error printed and therefore how to solve it.
Can someone help me? thanks a lot
The text was updated successfully, but these errors were encountered: