Automated Author ProfileHöfer, Katharina
Max Planck Institute for Terrestrial Microbiology
Höfer, Katharina
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 4 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
This repository complements the book chapter “Utilizing Golden Gate Assembly to Streamline CRISPR-Cas/NgTET-Based Phage Mutagenesis” by Nadiia Pozhydaieva and Katharina Höfer in “Methods in Molecular Biology” (in publishing). It contains the plasmids used for Golden Gate cloning as outlined in the approach. Golden Gate assembly is used to facilitate the exchange of donor DNA sequences (DNA sequences, that are introduced to phage genome upon mutagenesis), to streamline the mutagenesis process and rapidly customize it for various targets. Within this system, the donor DNA is integrated downstream of the gene for NgTET dioxygenase. The latter is crucial for the efficient engineering of phages with extensive cytosine DNA modifications.
Authors
- Pozhydaieva, Nadiia ;
- Höfer, Katharina
This repository complements the book chapter “Utilizing Golden Gate Assembly to Streamline CRISPR-Cas/NgTET-Based Phage Mutagenesis” by Nadiia Pozhydaieva and Katharina Höfer in “Methods in Molecular Biology” (in publishing). It contains the plasmids used for Golden Gate cloning as outlined in the approach. Golden Gate assembly is used to facilitate the exchange of donor DNA sequences (DNA sequences, that are introduced to phage genome upon mutagenesis), to streamline the mutagenesis process and rapidly customize it for various targets. Within this system, the donor DNA is integrated downstream of the gene for NgTET dioxygenase. The latter is crucial for the efficient engineering of phages with extensive cytosine DNA modifications.
Authors
- Pozhydaieva, Nadiia ;
- Höfer, Katharina
Supplementary Material 2
Authors
- Yousefi, Mohammad Hashem ;
- Wagemans, Jeroen ;
- Shekarforoush, Seyed Shahram ;
- Vallino, Marta ;
- Pozhydaieva, Nadiia ;
- Höfer, Katharina ;
- Lavigne, Rob ;
- Hosseinzadeh, Saeid
Supplementary Material 2
Authors
- Yousefi, Mohammad Hashem ;
- Wagemans, Jeroen ;
- Shekarforoush, Seyed Shahram ;
- Vallino, Marta ;
- Pozhydaieva, Nadiia ;
- Höfer, Katharina ;
- Lavigne, Rob ;
- Hosseinzadeh, Saeid