Closed peterk87 closed 2 years ago
Reads should be merged for the same sample whether they are from single FASTQ files or directories containing one or more FASTQ files:
/path/to/run1/fastq_pass/barcode01
/path/to/run2/fastq_pass/barcode09
/path/to/S1.run3.fq.gz
All reads for sample S1 should be merged into a single FASTQ file prior to further analysis.
Reads should be merged for the same sample whether they are from single FASTQ files or directories containing one or more FASTQ files:
/path/to/run1/fastq_pass/barcode01/path/to/run2/fastq_pass/barcode09/path/to/S1.run3.fq.gzAll reads for sample S1 should be merged into a single FASTQ file prior to further analysis.