mkdir fastq_multx_output-1 ./fastq-multx/fastq-multx -B barcode.txt -m 1 -b itaq.1.fastq itaq.2.fastq -o %.R1.fastq -o %.R2.fastq # 因为桥式PCR测序过程中双端序列方向不一定一致,因此需要颠倒两测序文件进行二次拆分 mkdir fastq_multx_output-2 ./fastq-multx/fastq-multx -B barcode.tx...
git clone https://github.com/brwnj/fastq-multx cd fastq-multx make Sequences are sometimes output to STDOUT in a different order on OS X versus Redhat, therefore some tests may fail. Example Usage Single index fastq-multx -B barcodes.tsv -m 0 \ Undetermined_S0_L001_I1_001.fastq.gz ...