1. Annotation and evaluation of base editing outcomes in multiple cell types using CRISPRbase. Issue Volume 51:Issue D1(2023) (9th November 2022) Authors: Fan, Jibiao; Shi, Leisheng; Liu, Qi; Zhu, Zhipeng; Wang, Fan; Song, Runxian; Su, Jimeng; Zhou, Degui; Chen, Xiao; Li, Kailong; Xue, Lixiang; Sun, Lichao; Mao, Fengbiao Journal: Nucleic acids research Issue: Volume 51:Issue D1(2023) Page Start: D1249 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CircleBase: an integrated resource and analysis platform for human eccDNAs. Issue Volume 50:Issue D1(2022) (18th November 2021) Authors: Zhao, Xiaolu; Shi, Leisheng; Ruan, Shasha; Bi, Wenjian; Chen, Yifan; Chen, Lin; Liu, Yifan; Li, Mingkun; Qiao, Jie; Mao, Fengbiao Journal: Nucleic acids research Issue: Volume 50:Issue D1(2022) Page Start: D72 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CirGRDB: a database for the genome-wide deciphering circadian genes and regulators. Issue Volume 46:Issue D1(2018) (20th October 2017) Authors: Li, Xianfeng; Shi, Leisheng; Zhang, Kun; Wei, Wenqing; Liu, Qi; Mao, Fengbiao; Li, Jinchen; Cai, Wanshi; Chen, Huiqian; Teng, Huajing; Li, Jiada; Sun, Zhongsheng Journal: Nucleic acids research Issue: Volume 46:Issue D1(2018) Page Start: D64 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Comprehensive evaluation of computational methods for predicting cancer driver genes. Issue 2 (17th January 2022) Authors: Shi, Xiaohui; Teng, Huajing; Shi, Leisheng; Bi, Wenjian; Wei, Wenqing; Mao, Fengbiao; Sun, Zhongsheng Journal: Briefings in bioinformatics Issue: Volume 23:Issue 2(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Corrigendum to: Genomic Diversity of Severe Acute Respiratory Syndrome–Coronavirus 2 in Patients With Coronavirus Disease 2019. (13th November 2021) Authors: Shen, Zijie; Xiao, Yan; Kang, Lu; Ma, Wentai; Shi, Leisheng; Zhang, Li; Zhou, Zhuo; Yang, Jing; Zhong, Jiaxin; Yang, Donghong; Guo, Li; Zhang, Guoliang; Li, Hongru; Xu, Yu; Chen, Mingwei; Gao, Zhancheng; Wang, Jianwei; Ren, Lili; Li, Mingkun Journal: Clinical infectious diseases Issue: Volume 73:Number 12(2021) Page Start: 2374 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genomic Diversity of Severe Acute Respiratory Syndrome–Coronavirus 2 in Patients With Coronavirus Disease 2019. (9th March 2020) Authors: Shen, Zijie; Xiao, Yan; Kang, Lu; Ma, Wentai; Shi, Leisheng; Zhang, Li; Zhou, Zhuo; Yang, Jing; Zhong, Jiaxin; Yang, Donghong; Guo, Li; Zhang, Guoliang; Li, Hongru; Xu, Yu; Chen, Mingwei; Gao, Zhancheng; Wang, Jianwei; Ren, Lili; Li, Mingkun Journal: Clinical infectious diseases Issue: Volume 71:Number 15(2020) Page Start: 713 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. OncoBase: a platform for decoding regulatory somatic mutations in human cancers. Issue Volume 47:Issue D1(2019) (16th November 2018) Authors: Li, Xianfeng; Shi, Leisheng; Wang, Yan; Zhong, Jianing; Zhao, Xiaolu; Teng, Huajing; Shi, Xiaohui; Yang, Haonan; Ruan, Shasha; Li, MingKun; Sun, Zhong Sheng; Zhan, Qimin; Mao, Fengbiao Journal: Nucleic acids research Issue: Volume 47:Issue D1(2019) Page Start: D1044 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Performance evaluation of pathogenicity-computation methods for missense variants. Issue 15 (28th July 2018) Authors: Li, Jinchen; Zhao, Tingting; Zhang, Yi; Zhang, Kun; Shi, Leisheng; Chen, Yun; Wang, Xingxing; Sun, Zhongsheng Journal: Nucleic acids research Issue: Volume 46:Issue 15(2018) Page Start: 7793 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. VarCards: an integrated genetic and clinical database for coding variants in the human genome. Issue Volume 46:Issue D1(2018) (3rd November 2017) Authors: Li, Jinchen; Shi, Leisheng; Zhang, Kun; Zhang, Yi; Hu, Shanshan; Zhao, Tingting; Teng, Huajing; Li, Xianfeng; Jiang, Yi; Ji, Liying; Sun, Zhongsheng Journal: Nucleic acids research Issue: Volume 46:Issue D1(2018) Page Start: D1039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Vitamin D‐related genes are subjected to significant de novo mutation burdens in autism spectrum disorder. Issue 5 (13th April 2017) Authors: Li, Jinchen; Wang, Lin; Yu, Ping; Shi, Leisheng; Zhang, Kun; Sun, Zhong Sheng; Xia, Kun Journal: American journal of medical genetics Issue: Volume 174:Issue 5(2017) Page Start: 568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗