Feasibility of xpore to work on non-nanopore RNA-seq data #95
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Dear Dr. GÖKE: I read with great interest your xpore application published in Nat Biotech to evaluate differential RNA modification using nanopore RNA-seq data. I am wondering if we can use xpore to analyze the other RNA-seq data generated by other sequencer platform such as HiSeq 2000 by converting the fastq (acquired from other sequencing platforms) to fast5 files (via other software such as fast5seek;https://github.com/mbhall88/fast5seek)? Or do you have some software we can apply (rather than fast5seek) to do the conversion from fastq to fast5 files for xpore application? Thank you for your support. Yong-Bi Fu |
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Replies: 1 comment
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Dear Yong-Bi Fu, Thanks for your interest in our work! xPore requires data that was processed by Nanopolish as input, so anything that works with Nanopolish would work with xPore. I am not aware of a software that translates fastq into fast5 for such a purpose, so in practice I believe xPore might currently only work with Nanopore direct RNA-Seq data. Thanks |
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Dear Yong-Bi Fu,
Thanks for your interest in our work! xPore requires data that was processed by Nanopolish as input, so anything that works with Nanopolish would work with xPore. I am not aware of a software that translates fastq into fast5 for such a purpose, so in practice I believe xPore might currently only work with Nanopore direct RNA-Seq data.
Thanks
Jonathan