Automated Organization ProfileFraunhofer-Institut fuer angewandte Informationstechnik FIT
Fraunhofer-Institut fuer angewandte Informationstechnik FIT
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets in this organization
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the organization's datasets
Total Mentions
Total mentions of the organization'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: 0.9 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Two datasets in HDF5 formats used for illustrating some quantitative data analysis methods.CCD_calibration.hdf5: Imago/SensiCam CCD camera (Till Photonics) calibration data set. Fluorescence measurments were made using a fluorescent plastic slide. 10 exposure times from 10 to 100 ms (each making an HDF5 group) were used. For each exposure time 100 exposures were performed (with 200 ms between each). The fluorescence measured in each of the 60 x 80 pixels of the camera are stored in the stack data set of each group. The time data set (a vector) of each group contains the time at which each illumination was done. These recordings were done by Andreas Pippow (Kloppenburg Laboratory Cologne University, http://cecad.uni-koeln.de/Prof-Peter-Kloppenburg.82.0.html). They were used in: Sébastien Joucla, Andreas Pippow, Peter Kloppenburg and Christophe Pouzat (2010) Quantitative estimation of calcium dynamics from ratiometric measurements: A direct, non-ratioing, method. Journal of Neurophysiology 103: 1130-1144.Data_POMC.hdf5: POMC data set recorded by Andreas Pippow (Kloppenburg Laboratory Cologne University, http://cecad.uni-koeln.de/Prof-Peter-Kloppenburg.82.0.html). 168 measurements performed with a CCD camera recording Fura-2 fluorescence (excitation wavelength: 340 nm). The size of the CCD chip is 60 x 80 pixels. A stimulation (depolarization induced calcium entry) comes at time 527. Details about this data set can be found in: Joucla et al (2013) Estimating background-subtracted fluorescence transients in calcium imaging experiments: A quantitative approach. Cell Calcium. 54 (2): 71-85.
Authors
- Pouzat, Christophe ;
- Pippow, Andreas ;
- Kloppenburg, Peter
Two datasets in HDF5 formats used for illustrating some quantitative data analysis methods.CCD_calibration.hdf5: Imago/SensiCam CCD camera (Till Photonics) calibration data set. Fluorescence measurments were made using a fluorescent plastic slide. 10 exposure times from 10 to 100 ms (each making an HDF5 group) were used. For each exposure time 100 exposures were performed (with 200 ms between each). The fluorescence measured in each of the 60 x 80 pixels of the camera are stored in the stack data set of each group. The time data set (a vector) of each group contains the time at which each illumination was done. These recordings were done by Andreas Pippow (Kloppenburg Laboratory Cologne University, http://cecad.uni-koeln.de/Prof-Peter-Kloppenburg.82.0.html). They were used in: Sébastien Joucla, Andreas Pippow, Peter Kloppenburg and Christophe Pouzat (2010) Quantitative estimation of calcium dynamics from ratiometric measurements: A direct, non-ratioing, method. Journal of Neurophysiology 103: 1130-1144.Data_POMC.hdf5: POMC data set recorded by Andreas Pippow (Kloppenburg Laboratory Cologne University, http://cecad.uni-koeln.de/Prof-Peter-Kloppenburg.82.0.html). 168 measurements performed with a CCD camera recording Fura-2 fluorescence (excitation wavelength: 340 nm). The size of the CCD chip is 60 x 80 pixels. A stimulation (depolarization induced calcium entry) comes at time 527. Details about this data set can be found in: Joucla et al (2013) Estimating background-subtracted fluorescence transients in calcium imaging experiments: A quantitative approach. Cell Calcium. 54 (2): 71-85.
Authors
- Pouzat, Christophe ;
- Pippow, Andreas ;
- Kloppenburg, Peter