Automated Author ProfileWillis, Joseph
Willis, Joseph
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: 1.3 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Cohorts, ethnicity, and tumor stage of samples used for WES, SNP array, and qPCR. Table S2. Regions with significant copy-number alterations, as detected by ENVE, in the 30 AA CRC WES cases. Table S3. Regions with significant copy-number alterations, as detected by ENVE, in the 30 predominantly late-stage Caucasian TCGA CRC WES cases. Table S4. Recurrent somatic copy-number altered regions in the 30 AA CRC WES cases estimated by GISTIC. Table S5. Recurrent focal copy-number amplifications and deletions in the 30 AA CRC WES cases estimated by GISTIC. Table S6. Chromosomal arm-level sCNA frequencies in AA and TCGA CRCs estimated by GISTIC. (XLSX 535 kb)
Authors
- Varadan, Vinay ;
- Salendra Singh ;
- Nosrati, Arman ;
- Lakshmeswari Ravi ;
- Lutterbaugh, James ;
- Barnholtz-Sloan, Jill ;
- Markowitz, Sanford ;
- Willis, Joseph ;
- Kishore Guda
Cohorts, ethnicity, and tumor stage of samples used for WES, SNP array, and qPCR. Table S2. Regions with significant copy-number alterations, as detected by ENVE, in the 30 AA CRC WES cases. Table S3. Regions with significant copy-number alterations, as detected by ENVE, in the 30 predominantly late-stage Caucasian TCGA CRC WES cases. Table S4. Recurrent somatic copy-number altered regions in the 30 AA CRC WES cases estimated by GISTIC. Table S5. Recurrent focal copy-number amplifications and deletions in the 30 AA CRC WES cases estimated by GISTIC. Table S6. Chromosomal arm-level sCNA frequencies in AA and TCGA CRCs estimated by GISTIC. (XLSX 535 kb)
Authors
- Varadan, Vinay ;
- Salendra Singh ;
- Nosrati, Arman ;
- Lakshmeswari Ravi ;
- Lutterbaugh, James ;
- Barnholtz-Sloan, Jill ;
- Markowitz, Sanford ;
- Willis, Joseph ;
- Kishore Guda