friend1ws / nanomonsv

SV detection tool for nanopore sequence reads
GNU General Public License v3.0
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about compare with short read SV in paper #25

Closed charliechen912ilovbash closed 2 years ago

charliechen912ilovbash commented 2 years ago

Hi, Could you describe a little bit about how you compare with short read sequencing detected SV in the paper? Like what is the margin (e.g. 20bp) to decide two breakpoint are closed enough to consider as the same SV. Thanks

friend1ws commented 2 years ago

In the paper, I used three categories; Detected, Partially detected, Not detected. Detected: Both the breakpoints and their directions match an SV detected by the short-read sequence platform within the margin of 30bp. Partially detected: One of the breakpoints matches an SV detected by the short-read sequence platform within the margin of 50bp. This applies often to LINE1 transduction, where they are usually identified as translocation in the short-read platform whereas it is identified as an insertion in the long-read. Not detected: Otherwise.

charliechen912ilovbash commented 2 years ago

Thanks for answering. So in the Figure 2b, the red parts (detected by both short and long read) are Detected + Partially detected ?

friend1ws commented 2 years ago

Thank you! I have never been asked this question by reviewers. But you are right. The red parts in Figure2b are Detected + Partially detected.

charliechen912ilovbash commented 2 years ago

I understood, thank you very much for answering!