Automated Author ProfileLi, Yue
McGill University
Li, Yue
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: 3.5 (sum of 3 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
This dataset contains the Linkage Disequilibrium (LD) matrices that were used in the analyses described in the manuscript: Fast and Accurate Bayesian Polygenic Risk Modeling with Variational Inference
Shadi Zabad, Simon Gravel, Yue Li
McGill University LD matrices record the SNP-by-SNP correlations in a given sample of individuals from a general population. In this case, we threshold the matrices so that we only record the correlations between SNPs that are at most 3 centi Morgan apart. These matrices record the SNP correlations in a random sample of 50,000 individuals from the White British cohort in the UK Biobank dataset. There is one matrix per autosomal chromosome (chr_1, chr_2, ..., chr_22). The matrices are stored in Zarr format, a chunked on-disk array storage format that allows for multi-threaded read and write access. To access these matrices, consult the codebase of magenpy, our custom python package with special data structures for processing these LD matrices. UPDATE (03/09/2022): We updated the matrices to add the reference allele attribute (A2) and we also now have one tar archive per chromosome.
Authors
- Zabad, Shadi ;
- Gravel, Simon ;
- Li, Yue
This dataset contains the Linkage Disequilibrium (LD) matrices that were used in the analyses described in the manuscript: Fast and Accurate Bayesian Polygenic Risk Modeling with Variational Inference
Shadi Zabad, Simon Gravel, Yue Li
McGill University LD matrices record the SNP-by-SNP correlations in a given sample of individuals from a general population. In this case, we threshold the matrices so that we only record the correlations between SNPs that are at most 3 centi Morgan apart. These matrices record the SNP correlations in a random sample of 50,000 individuals from the White British cohort in the UK Biobank dataset. There is one matrix per autosomal chromosome (chr_1, chr_2, ..., chr_22). The matrices are stored in Zarr format, a chunked on-disk array storage format that allows for multi-threaded read and write access. To access these matrices, consult the codebase of magenpy, our custom python package with special data structures for processing these LD matrices. UPDATE (03/09/2022): We updated the matrices to add the reference allele attribute (A2) and we also now have one tar archive per chromosome.
Authors
- Zabad, Shadi ;
- Gravel, Simon ;
- Li, Yue
This dataset contains the Linkage Disequilibrium (LD) matrices that were used in the analyses described in the manuscript: Fast and Accurate Bayesian Polygenic Risk Modeling with Variational Inference
Shadi Zabad, Simon Gravel, Yue Li
McGill University LD matrices record the SNP-by-SNP correlations in a given sample of individuals from a general population. In this case, we threshold the matrices so that we only record the correlations between SNPs that are at most 3 centi Morgan apart. These matrices record the SNP correlations in a random sample of 50,000 individuals from the White British cohort in the UK Biobank dataset. There is one matrix per autosomal chromosome (chr_1, chr_2, ..., chr_22). The matrices are stored in Zarr format, a chunked on-disk array storage format that allows for multi-threaded read and write access. To access these matrices, consult the codebase of magenpy, our custom python package with special data structures for processing these LD matrices.
Authors
- Zabad, Shadi ;
- Gravel, Simon ;
- Li, Yue