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I used Calib to deduplicate my paired end reads. calib -f S1_R1.fastq -r S1_R2.fastq -o S1_Calib. -l1 17 -l2 0
I have 8 bases index and 9 bases barcode attached to R1 while nothing attached to R2. Now, After running Calib and calib_cons, I noticed that the 17 bases of index+barcode is still attached to my reads. Is there a way to strip this?
Thanks!
The text was updated successfully, but these errors were encountered:
Note: Calib should work find with index+barcode but it might be an overkill. Consider splitting the reads by sample index first, and then running each sample separately with Calib.
Hello,
I used Calib to deduplicate my paired end reads.
calib -f S1_R1.fastq -r S1_R2.fastq -o S1_Calib. -l1 17 -l2 0
I have 8 bases index and 9 bases barcode attached to R1 while nothing attached to R2. Now, After running Calib and calib_cons, I noticed that the 17 bases of index+barcode is still attached to my reads. Is there a way to strip this?
Thanks!
The text was updated successfully, but these errors were encountered: