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The current implementation assumes paired end reads with inward orientation. And that information is used in distinguishing discordant reads with concordant, which affects genome segmentation but not rearrangement. For ISO-seq, the reads setting should be different, and requires a different implement of parsing reads. So short answer is I don't think it will run correctly on ISO-seq now. But I would like to look into ISO-reads alignment, and implement parsing long reads in the future.
We have ISO-seq alignments using gmap2, Will squid run on these data?
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