We read every piece of feedback, and take your input very seriously.
To see all available qualifiers, see our documentation.
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
I have the following script provided by BGI:
./iTools Fqtools splitpool -InFq1 file1.fq.gz -InFq2 file2.fq.gz -Index index.lst -Flag enzyme.txt -MisMatch -OutDir split/
What is the default setting for MisMatch?
MisMatch
Are there other options available?
The text was updated successfully, but these errors were encountered:
Also, what are the required file formatting for the -Flag input file and the -Index input file?
-Flag
-Index
Sorry, something went wrong.
-Flag the file with enzyme specific sequence such EcoRI seq is : AATTC -Index file with sample and barcodes [sample_ID sampleIndex ]
iTools Fqtools splitpool -InFq1 In_1.fq.gz -InFq2 In_1.fq.gz -Flag enzyme.seq -Index sample.index -OutDir OUTDir/ -MisMatch
cat enzyme.seq AATTC
head -4 sample.index S001 TGCGA S002 GGTTGT S003 ACGTGTT S004 ACAGGGAA @kubu4
No branches or pull requests
I have the following script provided by BGI:
./iTools Fqtools splitpool
-InFq1 file1.fq.gz
-InFq2 file2.fq.gz
-Index index.lst
-Flag enzyme.txt
-MisMatch
-OutDir split/
What is the default setting for
MisMatch
?Are there other options available?
The text was updated successfully, but these errors were encountered: