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Hi,
I want to remove adapters and demultiplex by barcode a couple of paired-end fastq files
First this basic command works fine so it means my files are likely to suit with flexbar usage:
flexbar -r $R1_fastq -b $Tags
But when i tried the following command:
flexbar -r $R1_fastq -p $R2_fastq -b $Tags -b2 $Tags -a $Primer_F -a2 $Primer_R -at 0.1 -t 02_demultiplex/ -n 4
I got the following message error:
________ __ / ____/ /__ _ __/ /_ ____ ______ / /_ / / _ \| |/ / __ \/ __ `/ ___/ / __/ / / __/> </ /_/ / /_/ / / /_/ /_/\___/_/|_/_.___/\__,_/_/ Flexbar - flexible barcode and adapter removal, version 2.5 Local time: Wed Dec 4 14:16:16 2019 Target name: 02_demultiplex/test/02_flexbar/grinder_teleo1 File type: fastq Reads file: /share/reservebenefit/working/Input_data/Outputs/grinder_teleo1/grinder_teleo1_R1.fastq Reads file 2: /share/reservebenefit/working/Input_data/Outputs/grinder_teleo1/grinder_teleo1_R2.fastq (paired run) Barcode file: /share/reservebenefit/working/pierre/eDNA--benchmark_pipelines/02_demultiplex/Tags.fasta Barcode file 2: /share/reservebenefit/working/pierre/eDNA--benchmark_pipelines/02_demultiplex/Tags.fasta Adapter file: /share/reservebenefit/working/pierre/eDNA--benchmark_pipelines/02_demultiplex/Primer_F.fasta Adapter file 2: /share/reservebenefit/working/pierre/eDNA--benchmark_pipelines/02_demultiplex/Primer_R.fasta threads: 4 max-uncalled: 0 min-read-length: 18 barcode-trim-end: ANY barcode-threshold: 1 barcode-match: 1 barcode-mismatch: -1 barcode-gap: -9 adapter-trim-end: RIGHT adapter-min-overlap: 3 adapter-threshold: 0.1 adapter-match: 1 adapter-mismatch: -1 adapter-gap: -6 Barcode: Sequence: S1-01 AACAAGCC S1-02 TGAGAGCT S1-03 ACAACCGA [...] S29-10 CTTGTGAC S29-11 TCTGTTCG S29-12 ACCAGTAC Barcode2: Sequence: S1-01 AACAAGCC S1-02 TGAGAGCT S1-03 ACAACCGA [...] S29-10 CTTGTGAC S29-11 TCTGTTCG S29-12 ACCAGTAC File reading error occured.
Do you have any idea what the problem is?
The text was updated successfully, but these errors were encountered:
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Hi,
I want to remove adapters and demultiplex by barcode a couple of paired-end fastq files
First this basic command works fine so it means my files are likely to suit with flexbar usage:
But when i tried the following command:
I got the following message error:
Do you have any idea what the problem is?
The text was updated successfully, but these errors were encountered: