Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders

NPJ Genom Med. 2021 Oct 12;6(1):88. doi: 10.1038/s41525-021-00251-3.

Joseph T Shieh^#^{1

2}, Monica Penon-Portmann^#^{3

4}, Karen H Y Wong^#⁵, Michal Levy-Sakin⁵, Michelle Verghese⁵, Anne Slavotinek^{3

4}, Renata C Gallagher^{3

4}, Bryce A Mendelsohn⁴, Jessica Tenney⁴, Daniah Beleford⁴, Hazel Perry⁴, Stephen K Chow⁵, Andrew G Sharo⁶, Steven E Brenner⁷, Zhongxia Qi⁸, Jingwei Yu⁸, Ophir D Klein^{3

4

9}, David Martin¹⁰, Pui-Yan Kwok^{3

5

11}, Dario Boffelli¹⁰

¹ Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA. [email protected].
² Division of Medical Genetics, Pediatrics, Benioff Children's Hospital, University of California San Francisco, San Francisco, CA, USA. [email protected].
³ Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
⁴ Division of Medical Genetics, Pediatrics, Benioff Children's Hospital, University of California San Francisco, San Francisco, CA, USA.
⁵ Cardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
⁶ Biophysics Graduate Group, University of California Berkeley, Berkeley, CA, USA.
⁷ Department of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA, USA.
⁸ Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA, USA.
⁹ Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA, USA.
¹⁰ Children's Hospital Oakland Research Institute, Benioff Children's Hospital Oakland, University of California San Francisco, Oakland, CA, USA.
¹¹ Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.

^# Contributed equally.

No abstract available

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