Automated Author ProfilePeacock, Anna F. A.
Peacock, Anna F. A.
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: 1.9 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
A high-density transposon library constructed in BW25113 was grown in the absence or presence of 0.25 mM or 0.5 mM sodium azide. In the case of the 0 mM and 0.25 mM samples, cells were grown until OD600 = 1.0. In the case of of the 0.5 mM sodium azide sample, the cells were grown to OD600 = 0.9, at which point the cells stopped growing exponentially. The location of the transposons after growth was determined using Illumina sequecing. Libraries were prepared using arbirary PCR and sequenced using single-end reads. Reads were then processed an aligned to the genome sequence for Escherichia coli K-12 strain W3110 (NCBI accession AP009048.1). Please see associated manuscript at BiorXiv for a more detailed description of the experiment.
Authors
- Huber, Damon ;
- Jamshad, Mohammed ;
- Chandler, Rachael ;
- Jeeves, Mark ;
- Robinson, Ashley ;
- Alam, Farhana ;
- Smith, Tamar Cranford ;
- Anokhi Shah ;
- Daubney, Oliver ;
- Dunne, Karl A. ;
- Nabi, Naomi ;
- Aadil Iqbal ;
- Peacock, Anna F. A. ;
- Lovett, Janet E. ;
- Knowles, Timothy ;
- Henderson, Ian
A high-density transposon library constructed in BW25113 was grown in the absence or presence of 0.25 mM or 0.5 mM sodium azide. In the case of the 0 mM and 0.25 mM samples, cells were grown until OD600 = 1.0. In the case of of the 0.5 mM sodium azide sample, the cells were grown to OD600 = 0.9, at which point the cells stopped growing exponentially. The location of the transposons after growth was determined using Illumina sequecing. Libraries were prepared using arbirary PCR and sequenced using single-end reads. Reads were then processed an aligned to the genome sequence for Escherichia coli K-12 strain W3110 (NCBI accession AP009048.1). Please see associated manuscript at BiorXiv for a more detailed description of the experiment.
Authors
- Huber, Damon ;
- Jamshad, Mohammed ;
- Chandler, Rachael ;
- Jeeves, Mark ;
- Robinson, Ashley ;
- Alam, Farhana ;
- Smith, Tamar Cranford ;
- Anokhi Shah ;
- Daubney, Oliver ;
- Dunne, Karl A. ;
- Nabi, Naomi ;
- Aadil Iqbal ;
- Peacock, Anna F. A. ;
- Lovett, Janet E. ;
- Knowles, Timothy ;
- Henderson, Ian