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European Journal of Human Genetics : EJHG|December 6, 2017
Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk lociYu Zhang, Lifeng Tian, Patrick Sleiman, et al.Genome Research|February 27, 2023
Complex hierarchical structures in single-cell genomics data unveiled by deep hyperbolic manifold learningTian Tian, Cheng Zhong, Xiang Lin, et al.Biological Psychiatry|October 21, 2023
A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number VariationsXiao Chang, Huiqi Qu, Yichuan Liu, et al.Nature Communications|March 26, 2021
Model-based deep embedding for constrained clustering analysis of single cell RNA-seq dataTian Tian, Jie Zhang, Xiang Lin, et al.American Journal of Medical Genetics. Part A|February 6, 2019
Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrumChaya Murali, Dong Li, Katheryn Grand, et al.Genes|April 28, 2023
RNA Sequencing in Hypoxia-Adapted T98G Glioblastoma Cells Provides Supportive Evidence for IRE1 as a Potential Therapeutic TargetBrian E White, Yichuan Liu, Hakon Hakonarson, et al.Nature Methods|May 23, 2024
Dependency-aware deep generative models for multitasking analysis of spatial omics dataTian Tian, Jie Zhang, Xiang Lin, et al.Discovery Medicine|July 29, 2011
Convergent mechanisms of somatic mutations in polycythemia veraKai Wang, Sabina Swierczek, Kimberly Hickman, et al.Nucleic Acids Research|August 5, 2011
SNVer: a statistical tool for variant calling in analysis of pooled or individual next-generation sequencing dataZhi Wei, Wei Wang, Pingzhao Hu, et al.World Journal of Gastroenterology|November 5, 2013
Impact of exome sequencing in inflammatory bowel diseaseChristopher J Cardinale, Judith R Kelsen, Robert N Baldassano, et al.Pageof 91