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Xihao Li

Showing results (21-30 of 64) with videos related to

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American Journal of Human Genetics|April 16, 2019
Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing StudiesZilin Li, Xihao Li, Yaowu Liu, et al.
Bioinformatics (Oxford, England)|April 20, 2022
STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysisSheila M Gaynor, Kenneth E Westerman, Lea L Ackovic, et al.
American Journal of Human Genetics|October 14, 2025
A scalable framework for identifying allelic series from summary statisticsZachary R McCaw, Jianhui Gao, Rounak Dey, et al.
Waste Management (New York, N.Y.)|May 8, 2026
Co-hydrothermal treatment of industrial solid wastes and organic material: Red mud weakens carbon stabilizationZhicheng Tan, Yu Zhang, Fangfang Li, et al.
Cancer Research|March 3, 2021
Association between Smoking History and Tumor Mutation Burden in Advanced Non-Small Cell Lung CancerXinan Wang, Biagio Ricciuti, Tom Nguyen, et al.
Human Molecular Genetics|June 9, 2025
Old vs. new local ancestry inference in HCHS/SOL: a comparative studyXueying Chen, Hao Wang, Iris Broce, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
Old vs. New Local Ancestry Inference in HCHS/SOL: A Comparative StudyXueying Chen, Hao Wang, Iris Broce, et al.
American Journal of Human Genetics|February 26, 2022
A multi-dimensional integrative scoring framework for predicting functional variants in the human genomeXihao Li, Godwin Yung, Hufeng Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Rare coding and noncoding variants map 1,342 diseases and biomarkers in 490,549 whole genomesYuxin Yuan, Yuanyuan Guan, Yannuo Feng, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Streamlining Large-Scale Genomic Data Management: Insights from the UK Biobank Whole-Genome Sequencing DataXihao Li, Andrew R Wood, Yuxin Yuan, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|April 16, 2019
Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing StudiesZilin Li, Xihao Li, Yaowu Liu, et al.
Bioinformatics (Oxford, England)|April 20, 2022
STAAR workflow: a cloud-based workflow for scalable and reproducible rare variant analysisSheila M Gaynor, Kenneth E Westerman, Lea L Ackovic, et al.
American Journal of Human Genetics|October 14, 2025
A scalable framework for identifying allelic series from summary statisticsZachary R McCaw, Jianhui Gao, Rounak Dey, et al.
Waste Management (New York, N.Y.)|May 8, 2026
Co-hydrothermal treatment of industrial solid wastes and organic material: Red mud weakens carbon stabilizationZhicheng Tan, Yu Zhang, Fangfang Li, et al.
Cancer Research|March 3, 2021
Association between Smoking History and Tumor Mutation Burden in Advanced Non-Small Cell Lung CancerXinan Wang, Biagio Ricciuti, Tom Nguyen, et al.
Human Molecular Genetics|June 9, 2025
Old vs. new local ancestry inference in HCHS/SOL: a comparative studyXueying Chen, Hao Wang, Iris Broce, et al.
Biorxiv : the Preprint Server for Biology|February 20, 2025
Old vs. New Local Ancestry Inference in HCHS/SOL: A Comparative StudyXueying Chen, Hao Wang, Iris Broce, et al.
American Journal of Human Genetics|February 26, 2022
A multi-dimensional integrative scoring framework for predicting functional variants in the human genomeXihao Li, Godwin Yung, Hufeng Zhou, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Rare coding and noncoding variants map 1,342 diseases and biomarkers in 490,549 whole genomesYuxin Yuan, Yuanyuan Guan, Yannuo Feng, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Streamlining Large-Scale Genomic Data Management: Insights from the UK Biobank Whole-Genome Sequencing DataXihao Li, Andrew R Wood, Yuxin Yuan, et al.
Pageof 7