Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yichuan Liu

Showing results (41-50 of 95) with videos related to

Pageof 10
Sort By:
International Journal of Molecular Sciences|April 3, 2021
Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene ClustersYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Frontiers in Genetics|September 26, 2019
Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family TriosYichuan Liu, Xiao Chang, Joseph Glessner, et al.
Scientific Reports|September 18, 2020
Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian childrenYichuan Liu, Xiao Chang, Huiqi Qu, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variationYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Nucleic Acids Research|December 24, 2013
PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distributionYu Hu, Yichuan Liu, Xianyun Mao, et al.
American Journal of Medical Genetics. Part A|October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB geneTalal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.
Genes|March 6, 2021
Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American AncestryYichuan Liu, Xiao Chang, Hui-Qi Qu, et al.
Alzheimer'S Research & Therapy|December 19, 2025
Unsupervised machine learning integrates genomic variants and EMR to unravel mechanisms of brain hemorrhage and epilepsy as early indicators of alzheimer's in down syndromeYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 9, 2021
Competitive Coordination of Chloride and Fluoride Anions Towards Trivalent Lanthanide Cations (La<sup>3+</sup> and Nd<sup>3+</sup> ) in Molten SaltsShilin Jiang, Jianhui Lan, Lin Wang, et al.
Cancer Communications (London, England)|October 10, 2024
Deciphering protective genomic factors of tumor development in pediatric Down syndrome via deep learning approach to whole genome and RNA sequencingYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Pageof 10

Showing results (41-50 of 95) with videos related to

Sort By:
Pageof 10
International Journal of Molecular Sciences|April 3, 2021
Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene ClustersYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Frontiers in Genetics|September 26, 2019
Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family TriosYichuan Liu, Xiao Chang, Joseph Glessner, et al.
Scientific Reports|September 18, 2020
Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian childrenYichuan Liu, Xiao Chang, Huiqi Qu, et al.
Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variationYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Nucleic Acids Research|December 24, 2013
PennSeq: accurate isoform-specific gene expression quantification in RNA-Seq by modeling non-uniform read distributionYu Hu, Yichuan Liu, Xianyun Mao, et al.
American Journal of Medical Genetics. Part A|October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB geneTalal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.
Genes|March 6, 2021
Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American AncestryYichuan Liu, Xiao Chang, Hui-Qi Qu, et al.
Alzheimer'S Research & Therapy|December 19, 2025
Unsupervised machine learning integrates genomic variants and EMR to unravel mechanisms of brain hemorrhage and epilepsy as early indicators of alzheimer's in down syndromeYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 9, 2021
Competitive Coordination of Chloride and Fluoride Anions Towards Trivalent Lanthanide Cations (La<sup>3+</sup> and Nd<sup>3+</sup> ) in Molten SaltsShilin Jiang, Jianhui Lan, Lin Wang, et al.
Cancer Communications (London, England)|October 10, 2024
Deciphering protective genomic factors of tumor development in pediatric Down syndrome via deep learning approach to whole genome and RNA sequencingYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Pageof 10