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Berndt, S. I.

Publications and source records attributed to Berndt, S. I..

2 recordsLinked to original sources

LDscore: a scalable, Python 3-powered web platform for LD score regression analysis

Linkage disequilibrium score regression (LDSC) is an important analytical tool for quantifying heritability and estimating genetic correlations between complex traits. However, the LDSC original implementation relies on an outdated Python 2 framework and deploying the standard command-line tools requires significant setup, data access, and computational expertise, creating a barrier for many researchers. To overcome these limitations, we developed LDscore, a significant technical and accessibility upgraded version of LDSC that allows for rapid analysis of GWAS data. The core advancement is the recoding of the LDSC framework in Python 3, enabling computational optimization and ensuring long-term sustainability. Built on top of this improved foundation, LDscore is implemented as a free, publicly available web application integrated within the popular NCI LDlink framework. LDscore can accelerate scientific research by providing an intuitive graphical interface for heritability estimation, genetic correlation, and LD score calculation, including access to an expanded range of reference populations for online analysis. Notably, our results show that selecting the most appropriate reference population LD panel, even at the subcontinental ancestry group level, is essential for minimizing population stratification bias in heritability estimation. By leveraging cloud computing for superior scalability and eliminating the need for local installation, LDscore adheres to FAIR principles, improving access, traceability, and reproducibility across an expanded set of reference populations, and effectively widens access to researchers worldwide providing support for in-depth genetic analyses. Brief summaryLinkage disequilibrium score regression (LDSC), a widely-used method for quantifying heritability and genetic correlation, is limited by an outdated Python 2 framework and complex command-line deployment. We developed LDscore, a significant technical upgrade built on Python 3 for sustainability and computational optimization. LDscore is a free, cloud-based web application integrated into NCI LDlink. LDscore eliminates installation barriers, offering an intuitive interface for computing heritability estimates, LD scores, and genetic correlation. Crucially, LDscore expands the range of reference populations available in LDSC, which can reduce population-stratification-based bias. Leveraging cloud computing, LDscore accelerates and widens global researcher access to LDSC-based genetic computation. AvailabilityLDscore is freely available within LDlink at https://ldlink.nih.gov/ldscore. Source code for the updated LDSC Python3 framework is available at https://github.com/CBIIT/ldsc under the GNU General Public License v3.0 and the webtool code is at https://github.com/CBIIT/nci-webtools-dceg-linkage (webtool code) under the MIT license.

genomics↗

Physical activity and risks of breast and colorectal cancer: A Mendelian randomization analysis

Physical activity has been associated with lower risks of breast and colorectal cancer in epidemiological studies; however, it is unknown if these associations are causal or confounded. In two-sample Mendelian randomization analyses, using summary genetic data from the UK Biobank and GWA consortia, we found that a one standard deviation increment in average acceleration was associated with lower risks of breast cancer (odds ratio [OR]: 0.59, 95% confidence interval [CI]: 0.42 to 0.84, P-value=0.003) and colorectal cancer (OR: 0.66, 95% CI: 0.53 to 0.82, P-value=2*E-4). We found similar magnitude inverse associations by breast cancer subtype and by colorectal cancer anatomical site. Our results support a potentially causal relationship between higher physical activity levels and lower risks of breast cancer and colorectal cancer. Based on these data, the promotion of physical activity is probably an effective strategy in the primary prevention of these commonly diagnosed cancers.\n\nDisclaimerWhere authors are identified as personnel of the International Agency for Research on Cancer / World Health Organization, the authors alone are responsible for the views expressed in this article and they do not necessarily represent the decisions, policy or views of the International Agency for Research on Cancer / World Health Organization.

genetics↗