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Demultiplexing sample  #10

@nirwan1265

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@nirwan1265

I am trying to demultiplex the samples before the analysis to get samples first. This is the code:

java -jar /rsstu/users/r/rrellan/sara/nirwan_backup/ntanduk/BRBseqTools.jar Demultiplex -r1 /rsstu/users/r/rrellan/sara/RNA_Sequencing_raw/BZea_CLY23D1/NVS205B_RellanAlvarez/BZeaR2_S1_L004_R1_001.fastq.gz -r2 /rsstu/users/r/rrellan/sara/RNA_Sequencing_raw/BZea_CLY23D1/NVS205B_RellanAlvarez/BZeaR2_S1_L004_R2_001.fastq.gz -c /share/maize/ntanduk/BZea/rnaseq/barcodes.txt -p BU -UMI 14

this is my barcodes.txt

(base) [ntanduk@login02 rnaseq]$ more barcodes.txt 
Name	B1
B73_1	TACACTATAGCTAG	
B73_2	CAGACATGATAGAG
B73_3	TCTTGAACGACTAA
B73_4	ACCAACTTAGACAA
B73_5	CCATATTGAAGCAC
B73_6	TTCATGGTAGAGAG
B73_7	CACGTAGCTAGACG
B73_8	ATACGATGCTGCGC
B73_9	ACTTAAGGTCCAAC
B73_10	CTCTCAAGTCCTCC

This is my error:

Error while parsing R1 FastQ file
Read found in FastQ has length 151 while barcode pattern has length 28

I have UMI in my samples.

Any help is appreciated

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