- https://www.claretbio.com/products/srsly-umi
- https://www.claretbio.com/products/srsly-run
- https://github.com/claretbio/srslyumi
-
source /isilon/RnD/tools/bcbio_072619/env.sh
-
source /isilon/prodx/bcl2fastq/2.20.0.422/env.sh
-
srslyumi /scratch/ngs_run_data/Sequencing_Raw_Data/NovaSeqOutput/220411_A01690_0016_AHTWVGDRXY /scratch/ngs_run_data/Sequencing_Raw_Data/NovaSeqOutput/220411_A01690_0016_AHTWVGDRXY/Data/Intensities/BaseCalls/FASTQ
-
python library location:
/isilon/RnD/bcbio-tool-data/anaconda/lib/python3.6/site-packages/srslyumi/
- updating with
--no-lane-splitting
in/isilon/RnD/bcbio-tool-data/anaconda/lib/python3.6/site-packages/srslyumi/cli.py
- updating with
-
fix the UMI in the read name to be compatible with bcbio
- in the FASTQ folder, do
/isilon/RnD/tools/custom_script/wes/fastq_umi_fix.sh
- in the FASTQ folder, do