Automated Author ProfileQiao, Chang
0000-0002-0170-9877
Qiao, Chang
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: 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
This is LLS-SIM dataset of Fibrillar Center, which is a part of BioSR for LLS-SIM dataset (https://doi.org/10.5281/zenodo.14322457).BioSR for LLS-SIM is a biological image dataset acquired using our home-built lattice light-sheet structured illumination microscopy (LLS-SIM). It currently includes paired diffraction-limited LLSM and LLS-SIM images of a variety of biology structures, constituting a high-quality volumetric SR dataset. The BioSR for LLS-SIM dataset originates from our paper [Qiao, C., Li, Z., Wang, Z., Lin, Y., ... & Li, D. (2024). Fast adaptive super-resolution lattice light-sheet microscopy for rapid, long-term, near-isotropic subcellular imaging. bioRxiv, 2024-05], serving as the supplementary data to execute meta-training or other proposed deep-learning-based algorithms, which provides sources for the community to try our methods, replicate our results, and develop their own methods for super-resolution lattice light-sheet microscopy.The BioSR for LLS-SIM dataset includes 10 diverse task datasets from 10 distinct biological specimens (granular component, chromosomes, fibrillar center, fibrillarin, Lyso, MTs, F-actin in pollen tubes, inner mitochondrial membrane, ER in adherent Cos-7 cells and ER in mitotic Hela cells during metaphase). For each type of samples, we acquired raw LLS-SIM images from about 30-50 ROIs. For each ROI, five different levels of light intensity ranging from low to high fluorescence levels were acquired, and the images of the highest fluorescence level (i.e. the GT raw images) were reconstructed into high-quality GT LLS-SIM images via the conventional LLS-SIM reconstruction algorithm, which could be used as the groud truth in the training phase of deep-learning models.
Authors
- Qiao, Chang ;
- Lin, Yuhuan
This is LLS-SIM dataset of Fibrillar Center, which is a part of BioSR for LLS-SIM dataset (https://doi.org/10.5281/zenodo.14322457).BioSR for LLS-SIM is a biological image dataset acquired using our home-built lattice light-sheet structured illumination microscopy (LLS-SIM). It currently includes paired diffraction-limited LLSM and LLS-SIM images of a variety of biology structures, constituting a high-quality volumetric SR dataset. The BioSR for LLS-SIM dataset originates from our paper [Qiao, C., Li, Z., Wang, Z., Lin, Y., ... & Li, D. (2024). Fast adaptive super-resolution lattice light-sheet microscopy for rapid, long-term, near-isotropic subcellular imaging. bioRxiv, 2024-05], serving as the supplementary data to execute meta-training or other proposed deep-learning-based algorithms, which provides sources for the community to try our methods, replicate our results, and develop their own methods for super-resolution lattice light-sheet microscopy.The BioSR for LLS-SIM dataset includes 10 diverse task datasets from 10 distinct biological specimens (granular component, chromosomes, fibrillar center, fibrillarin, Lyso, MTs, F-actin in pollen tubes, inner mitochondrial membrane, ER in adherent Cos-7 cells and ER in mitotic Hela cells during metaphase). For each type of samples, we acquired raw LLS-SIM images from about 30-50 ROIs. For each ROI, five different levels of light intensity ranging from low to high fluorescence levels were acquired, and the images of the highest fluorescence level (i.e. the GT raw images) were reconstructed into high-quality GT LLS-SIM images via the conventional LLS-SIM reconstruction algorithm, which could be used as the groud truth in the training phase of deep-learning models.
Authors
- Qiao, Chang ;
- Lin, Yuhuan