Publication not explained

This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.

If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.

Featured Image

Read the Original

This page is a summary of: Use of whole genome sequencing to identify low-frequency mutations in COVID-19 patients treated with remdesivir, November 2022, Cold Spring Harbor Laboratory Press, DOI: 10.1101/2022.11.20.22282552.
You can read the full text:



The following have contributed to this page