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

Vitor Onuchic

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Plos Computational Biology|October 8, 2013
ToPS: a framework to manipulate probabilistic models of sequence dataAndré Yoshiaki Kashiwabara, Igor Bonadio, Vitor Onuchic, et al.
Nature Communications|February 19, 2015
Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAsViren Amin, R Alan Harris, Vitor Onuchic, et al.
Bioinformatics Advances|April 18, 2025
Benchmarking of germline copy number variant callers from whole genome sequencing data for clinical applicationsFrancisco M De La Vega, Sean A Irvine, Pavana Anur, et al.
Cell Reports|November 17, 2016
Epigenomic Deconvolution of Breast Tumors Reveals Metabolic Coupling between Constituent Cell TypesVitor Onuchic, Ryan J Hartmaier, David N Boone, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithmsSairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Nature Biotechnology|October 25, 2024
Comprehensive genome analysis and variant detection at scale using DRAGENSairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Science (New York, N.Y.)|August 25, 2018
Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory lociVitor Onuchic, Eugene Lurie, Ivenise Carrero, et al.
BMC Medical Genomics|October 25, 2024
Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease riskSairam Behera, Jonathan R Belyeu, Xiao Chen, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
Nature|February 20, 2015
Integrative analysis of 111 reference human epigenomes, Anshul Kundaje, Wouter Meuleman, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Plos Computational Biology|October 8, 2013
ToPS: a framework to manipulate probabilistic models of sequence dataAndré Yoshiaki Kashiwabara, Igor Bonadio, Vitor Onuchic, et al.
Nature Communications|February 19, 2015
Epigenomic footprints across 111 reference epigenomes reveal tissue-specific epigenetic regulation of lincRNAsViren Amin, R Alan Harris, Vitor Onuchic, et al.
Bioinformatics Advances|April 18, 2025
Benchmarking of germline copy number variant callers from whole genome sequencing data for clinical applicationsFrancisco M De La Vega, Sean A Irvine, Pavana Anur, et al.
Cell Reports|November 17, 2016
Epigenomic Deconvolution of Breast Tumors Reveals Metabolic Coupling between Constituent Cell TypesVitor Onuchic, Ryan J Hartmaier, David N Boone, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithmsSairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Nature Biotechnology|October 25, 2024
Comprehensive genome analysis and variant detection at scale using DRAGENSairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Science (New York, N.Y.)|August 25, 2018
Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory lociVitor Onuchic, Eugene Lurie, Ivenise Carrero, et al.
BMC Medical Genomics|October 25, 2024
Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease riskSairam Behera, Jonathan R Belyeu, Xiao Chen, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
Nature|February 20, 2015
Integrative analysis of 111 reference human epigenomes, Anshul Kundaje, Wouter Meuleman, et al.
Pageof 1