Hello,
I am doing a comparison of duplicated reads on Illumina NovaSeq vs MGI G400 by checking the distribution of reads on the flowcell....
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G400 fastq header description?
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trimming BGI adapters
Hello,
I have paired-end 100bp reads generated from BGI-seq 500. The sequencing center did some adapter removal trimming before delivering...
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Understanding the qmap bis-seq format
Hello,
I hoping somebody can help me to understand the qmap format, used to describe the bis-seq methylome data from recent papers. I downloaded...
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Just say hello (new guy from BGI Shenzhen,China)

Hi all !
My id here is "node"
and my name is Gentle Yang ("子江" in Chinese).
...