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

Shili Lin

Showing results (41-50 of 145) with videos related to

Pageof 15
Sort By:
Bioinformatics (Oxford, England)|May 23, 2014
FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triadsMeng Wang, Shili Lin
BMC Proceedings|December 19, 2009
Detection of imprinting and heterogeneous maternal effects on high blood pressure using Framingham Heart Study dataJingyuan Yang, Shili Lin
Genetic Epidemiology|September 1, 2020
Detecting X-linked common and rare variant effects in family-based sequencing studiesAsuman S Turkmen, Shili Lin
BMC Proceedings|December 19, 2014
Identifying rare variant associations in population-based and family-based designsAsuman S Turkmen, Shili Lin
Bioinformatics (Oxford, England)|January 23, 2015
GrammR: graphical representation and modeling of count data with application in metagenomicsDeepak Nag Ayyala, Shili Lin
Plos One|January 28, 2014
Blocking approach for identification of rare variants in family-based association studiesAsuman S Turkmen, Shili Lin
BMC Proceedings|March 1, 2012
Gene-based partial least-squares approaches for detecting rare variant associations with complex traitsAsuman S Turkmen, Shili Lin
Genetic Epidemiology|June 19, 2003
Linkage analysis with sequential imputationZachary Skrivanek, Shili Lin, Mark Irwin
Briefings in Bioinformatics|November 17, 2020
Are dropout imputation methods for scRNA-seq effective for scHi-C data?Chenggong Han, Qing Xie, Shili Lin
Biodata Mining|December 23, 2015
Network construction and structure detection with metagenomic count dataZhenqiu Liu, Shili Lin, Steven Piantadosi
Pageof 15

Showing results (41-50 of 145) with videos related to

Sort By:
Pageof 15
Bioinformatics (Oxford, England)|May 23, 2014
FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triadsMeng Wang, Shili Lin
BMC Proceedings|December 19, 2009
Detection of imprinting and heterogeneous maternal effects on high blood pressure using Framingham Heart Study dataJingyuan Yang, Shili Lin
Genetic Epidemiology|September 1, 2020
Detecting X-linked common and rare variant effects in family-based sequencing studiesAsuman S Turkmen, Shili Lin
BMC Proceedings|December 19, 2014
Identifying rare variant associations in population-based and family-based designsAsuman S Turkmen, Shili Lin
Bioinformatics (Oxford, England)|January 23, 2015
GrammR: graphical representation and modeling of count data with application in metagenomicsDeepak Nag Ayyala, Shili Lin
Plos One|January 28, 2014
Blocking approach for identification of rare variants in family-based association studiesAsuman S Turkmen, Shili Lin
BMC Proceedings|March 1, 2012
Gene-based partial least-squares approaches for detecting rare variant associations with complex traitsAsuman S Turkmen, Shili Lin
Genetic Epidemiology|June 19, 2003
Linkage analysis with sequential imputationZachary Skrivanek, Shili Lin, Mark Irwin
Briefings in Bioinformatics|November 17, 2020
Are dropout imputation methods for scRNA-seq effective for scHi-C data?Chenggong Han, Qing Xie, Shili Lin
Biodata Mining|December 23, 2015
Network construction and structure detection with metagenomic count dataZhenqiu Liu, Shili Lin, Steven Piantadosi
Pageof 15