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

BMC proceedings

Showing results (81-90 of 1,279) with videos related to

Pageof 128
Sort By:
BMC Proceedings|September 20, 2014
Integrative visual analysis of protein sequence mutationsNadezhda T Doncheva, Karsten Klein, John H Morris, et al.
BMC Proceedings|September 20, 2014
FixingTIM: interactive exploration of sequence and structural data to identify functional mutations in protein familiesTimothy Luciani, John Wenskovitch, Koonwah Chen, et al.
BMC Proceedings|September 20, 2014
Mu-8: visualizing differences between proteins and their familiesJohnathan D Mercer, Balaji Pandian, Alexander Lex, et al.
BMC Proceedings|September 20, 2014
Sequence Diversity Diagram for comparative analysis of multiple sequence alignmentsRyo Sakai, Jan Aerts
BMC Proceedings|March 1, 2012
Cell-based medicinal products and the development of GMP-compliant processes and manufacturingLuca Romagnoli, Ilaria Giuntini, Marta Galgano, et al.
BMC Proceedings|March 1, 2012
Population structure analysis using rare and common functional variantsTesfaye M Baye, Hua He, Lili Ding, et al.
BMC Proceedings|March 1, 2012
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 dataJenna Sykes, Lu Cheng, Wei Xu, et al.
BMC Proceedings|March 1, 2012
Improvement of stem cell performance by supplementation with metabolic enhancersAbi M Abitorabi, Christopher Wilcox
BMC Proceedings|March 1, 2012
A novel method to detect rare variants using both family and unrelated case-control dataTao Feng, Robert C Elston, Xiaofeng Zhu
BMC Proceedings|March 1, 2012
Combining effects from rare and common genetic variants in an exome-wide association study of sequence dataHugues Aschard, Weiliang Qiu, Bogdan Pasaniuc, et al.
Pageof 128

Showing results (81-90 of 1,279) with videos related to

Sort By:
Pageof 128
BMC Proceedings|September 20, 2014
Integrative visual analysis of protein sequence mutationsNadezhda T Doncheva, Karsten Klein, John H Morris, et al.
BMC Proceedings|September 20, 2014
FixingTIM: interactive exploration of sequence and structural data to identify functional mutations in protein familiesTimothy Luciani, John Wenskovitch, Koonwah Chen, et al.
BMC Proceedings|September 20, 2014
Mu-8: visualizing differences between proteins and their familiesJohnathan D Mercer, Balaji Pandian, Alexander Lex, et al.
BMC Proceedings|September 20, 2014
Sequence Diversity Diagram for comparative analysis of multiple sequence alignmentsRyo Sakai, Jan Aerts
BMC Proceedings|March 1, 2012
Cell-based medicinal products and the development of GMP-compliant processes and manufacturingLuca Romagnoli, Ilaria Giuntini, Marta Galgano, et al.
BMC Proceedings|March 1, 2012
Population structure analysis using rare and common functional variantsTesfaye M Baye, Hua He, Lili Ding, et al.
BMC Proceedings|March 1, 2012
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 dataJenna Sykes, Lu Cheng, Wei Xu, et al.
BMC Proceedings|March 1, 2012
Improvement of stem cell performance by supplementation with metabolic enhancersAbi M Abitorabi, Christopher Wilcox
BMC Proceedings|March 1, 2012
A novel method to detect rare variants using both family and unrelated case-control dataTao Feng, Robert C Elston, Xiaofeng Zhu
BMC Proceedings|March 1, 2012
Combining effects from rare and common genetic variants in an exome-wide association study of sequence dataHugues Aschard, Weiliang Qiu, Bogdan Pasaniuc, et al.
Pageof 128