Automated Author ProfileTay, Joshua
Tay, Joshua
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: 1.0 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Nasopharyngeal swabs from infected adults were obtained during the acute and late convalescent phase of SARS-CoV-2 infection and compared the expression of both genes with non-infected family household member contacts at the National University Hospital, Singapore. Viral inactivation was performed prior to RNA extraction, followed by cDNA synthesis using the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Thermo Fisher Scientific, Waltham, MA). RT-qPCR was performed to determine gene expression of ACE2 and TMPRSS2 against the housekeeping control 18S using the PerfeCTa SYBR® Green FastMix with Low ROX (Quantabio, Beverly, MA) and QuantStudio 5 Real-Time PCR system (Applied Biosystems, Thermo Fisher Scientific, Waltham, MA).
Authors
- Hui En Chen, Vannessa ;
- Tay, Joshua ;
- Gurung, Rijan ;
- Nair, Smeetha ;
- Tay, Douglas Jie Wen ;
- Tan, Kai Sen ;
- Foo, Roger ;
- Tambyah, Paul Anantharajah
Nasopharyngeal swabs from infected adults were obtained during the acute and late convalescent phase of SARS-CoV-2 infection and compared the expression of both genes with non-infected family household member contacts at the National University Hospital, Singapore. Viral inactivation was performed prior to RNA extraction, followed by cDNA synthesis using the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Thermo Fisher Scientific, Waltham, MA). RT-qPCR was performed to determine gene expression of ACE2 and TMPRSS2 against the housekeeping control 18S using the PerfeCTa SYBR® Green FastMix with Low ROX (Quantabio, Beverly, MA) and QuantStudio 5 Real-Time PCR system (Applied Biosystems, Thermo Fisher Scientific, Waltham, MA).
Authors
- Hui En Chen, Vannessa ;
- Tay, Joshua ;
- Gurung, Rijan ;
- Nair, Smeetha ;
- Tay, Douglas Jie Wen ;
- Tan, Kai Sen ;
- Foo, Roger ;
- Tambyah, Paul Anantharajah