Automated Author ProfileBu, Fengxiao
West China Hospital of Sichuan University0000-0002-4882-4856
Bu, Fengxiao
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 0.4 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Additional file 1: Table S1. List of 115 SNVs and three CNVs in SNPscan assay. Table S2. 157 hearing loss related genes included in the CDGC-HL panel. Table S3. 9,050 variants included in this study. Table S4. Allele frequency thresholds for variants could reach p-value<0.05 with different case sample size. Table S5. Variants in truth subset 1. Table S6. Variants in truth subset 2. Table S7. Variants in truth subset 3. Table S8. Evaluation metrics and positive likelihood ratio with different cutoffs in Truth Subset 1 and Truth Subset 3. Table S9. Summary of variants meeting the proposed PS4 thresholds. Table S10. The clinical and genetic findings of the 8 patients with upgraded P/LP variants. Table S11. CNVplex results of F3:II-1. Table S12. Correlation between PS4 and PM3 in the truth subset 3.
Authors
- Liu, Sihan ;
- Zhong, Mingjun ;
- Huang, Yu ;
- Zhang, Qian ;
- Chen, Ting ;
- Xu, Xiaofei ;
- Peng, Wan ;
- Wang, Xiaolu ;
- Feng, Xiaoshu ;
- Kang, Lu ;
- Lu, Yu ;
- Cheng, Jing ;
- Bu, Fengxiao ;
- Yuan, Huijun
Additional file 1: Table S1. List of 115 SNVs and three CNVs in SNPscan assay. Table S2. 157 hearing loss related genes included in the CDGC-HL panel. Table S3. 9,050 variants included in this study. Table S4. Allele frequency thresholds for variants could reach p-value<0.05 with different case sample size. Table S5. Variants in truth subset 1. Table S6. Variants in truth subset 2. Table S7. Variants in truth subset 3. Table S8. Evaluation metrics and positive likelihood ratio with different cutoffs in Truth Subset 1 and Truth Subset 3. Table S9. Summary of variants meeting the proposed PS4 thresholds. Table S10. The clinical and genetic findings of the 8 patients with upgraded P/LP variants. Table S11. CNVplex results of F3:II-1. Table S12. Correlation between PS4 and PM3 in the truth subset 3.
Authors
- Liu, Sihan ;
- Zhong, Mingjun ;
- Huang, Yu ;
- Zhang, Qian ;
- Chen, Ting ;
- Xu, Xiaofei ;
- Peng, Wan ;
- Wang, Xiaolu ;
- Feng, Xiaoshu ;
- Kang, Lu ;
- Lu, Yu ;
- Cheng, Jing ;
- Bu, Fengxiao ;
- Yuan, Huijun