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BGI-Qingdao / TGS-GapCloser

A gap-closing software tool that uses long reads to enhance genome assembly.
GNU General Public License v3.0
179 stars 13 forks source link

Using different reads to fill the gap in genome #87

Open DayTimeMouse opened 2 months ago

DayTimeMouse commented 2 months ago

Hi,

Thanks to develop this wonderful tool.

I want to ask that can I use different reads to fill the gap in genome? Because of having different reads, like HiFi reads, ONT reads.

Can I use HiFi reads to fill the gap first, then use ONT reads?

Best wishes.