DOES MGI SEQUENCING RESULT CONTAINS MULTIPLE FILES FOR SINGLE SAMPLE
HII.. I got a whole genome sequenced by MGI (short read sequencing). but instead of 2 files(read1 and read2) we got 4 different set of files for a single organism i.e. i got 4 pair of fastq files. i am new to BGseq. i wanted to know is it normal and how i can merge them into a single pair of files ???
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WouterDeCoster
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manaswiniparija3 •
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manaswiniparija3 •
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It would be helpful to show us the file names. You probably received data from multiple lanes, and you don't need to merge them before going further into the alignment step.