Correction to: Genome Biol 22, 297 (2021).

https://doi.org/10.1186/s13059-021-02513-w

Following publication of the original article [1], the authors identified an error in the author affiliations presented in additional file 1. The additional file has been updated and published in this correction.

The original article [1] has been corrected.

1. 1.

   Mei H, Zha Z, Wang W, Xie Y, Huang Y, Li W, et al. Surfaceome CRISPR screen identifies OLFML3 as a rhinovirus-inducible IFN antagonist. Genome Biol. 2021;22(1):297. https://doi.org/10.1186/s13059-021-02513-w.

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1. Hong Mei, Zhao Zha and Wei Wang contributed equally to this work.

Affiliations

1. Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, People’s Republic of China

   Hong Mei, Zhao Zha, Wei Wang, Yuege Huang, Wenping Li & Jia Liu

2. Department of Respiratory and Critical Care Medicine, Ruijin Hospital and Institutes of Respiratory Diseases, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China

   Yusang Xie & Jieming Qu

3. University of Chinese Academy of Sciences, Beijing, 100049, China

   Yuege Huang & Wenping Li

4. Research Laboratory of Clinical Virology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China

   Dong Wei & Xinxin Zhang

5. Shanghai Clinical Research and Trial Center, Shanghai, 201210, People’s Republic of China

   Jia Liu

6. State Key Laboratory of Respiratory Disease, Guangzhou Medical University, Guangzhou, 510182, Guangdong Province, China

   Jia Liu

7. Gene Editing Center, School of Life Science and Technology, ShanghaiTech University, Shanghai, 201210, People’s Republic of China

   Jia Liu

8. Guangzhou Laboratory, No. 9 XingDaoHuanBei Road, Guangzhou International Bio Island, Guangzhou, 510005, Guangdong Province, China

   Jia Liu

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Additional file 1: Fig. S1.

Construction of CRISPR genome-wide and surfaceome libraries. Fig. S2. Quality analyses of constructed genome-wide and surfaceome CRISPR libraries. Fig. S3. Evaluation of surfaceome and genome-wide CRISPR libraries. Fig. S4. Validation of the screening results. Fig. S5. Determination of gene modification efficiency. Fig. S6. Validation of the top 10 hits from surfaceome and genome-wide screens. Fig. S7. Construction and validation of single clones of ICAM-1^−/−, RAB5C^−/−, OLFML3^−/−, SLC4A7^−/− and ATP6AP1^−/+ H1-Hela cells. Fig. S8. Validation of the effects of ICAM-1, RAB5C and OLFML3 on RV infection, related to Fig. 3. Fig. S9. Dissection of the functions of RAB5C and OLFML3 in RV infection. Fig. S10. RNA-seq analyses of the effects of RAB5C knockout on RV infection. Fig. S11. RNA-Seq analyses of the effects of OLFML3 on RV infection (related to Fig. 4). Fig. S12. Bar plots showing RT-qPCR quantification of ISG expression in mock and OLML3−/− cells at 24 h post infection of RV-B14 (a) and RV-A16 (b) at an MOI of 2

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Mei, H., Zha, Z., Wang, W. et al. Correction: Surfaceome CRISPR screen identifies OLFML3 as a rhinovirus-inducible IFN antagonist. Genome Biol 22, 314 (2021). https://doi.org/10.1186/s13059-021-02534-5

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• Published: 15 November 2021

• DOI: https://doi.org/10.1186/s13059-021-02534-5

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