How to process Iso-seq subreads in fastq downloaed from NCBI SRA database ?
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19 months ago
2310691738 ▴ 10

The CCS software is capable of processing bam format files from the PacBio platform. However, I've noticed that many long-read datasets in the NCBI SRA database end with ".subread.fastq" extension, while CCS cannot utilize fastq files. How can this be addressed?

pacbio • 406 views
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