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Victoria Popic

Showing results (11-20 of 19) with videos related to

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Nature Methods|March 24, 2023
Cue: a deep-learning framework for structural variant discovery and genotypingVictoria Popic, Chris Rohlicek, Fabio Cunial, et al.
Genome Biology|May 7, 2015
Fast and scalable inference of multi-sample cancer lineagesVictoria Popic, Raheleh Salari, Iman Hajirasouliha, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2025
A Murine Database of Structural Variants Enables the Genetic Architecture of a Spontaneous Murine Lymphoma to be CharacterizedWenlong Ren, Zhuoqing Fang, Egor Dolzhenko, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 28, 2026
A Murine Database of Structural Variants Identifies A Candidate Gene for a Spontaneous Murine Lymphoma ModelWenlong Ren, Zhuoqing Fang, Egor Dolzhenko, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
CTAT-LR-fusion: accurate fusion transcript identification from long and short read isoform sequencing at bulk or single cell resolutionQian Qin, Victoria Popic, Houlin Yu, et al.
Genome Research|March 14, 2025
Accurate fusion transcript identification from long- and short-read isoform sequencing at bulk or single-cell resolutionQian Qin, Victoria Popic, Kirsty Wienand, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in DiseaseKwanho Kim, Zechuan Lin, Sean K Simmons, et al.
Nature Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
Accurate strand-specific long-read transcript isoform discovery and quantification at bulk, single-cell, and single-nucleus resolutionHoulin Yu, Christophe H Georgescu, Akanksha Khorgade, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Nature Methods|March 24, 2023
Cue: a deep-learning framework for structural variant discovery and genotypingVictoria Popic, Chris Rohlicek, Fabio Cunial, et al.
Genome Biology|May 7, 2015
Fast and scalable inference of multi-sample cancer lineagesVictoria Popic, Raheleh Salari, Iman Hajirasouliha, et al.
Biorxiv : the Preprint Server for Biology|January 27, 2025
A Murine Database of Structural Variants Enables the Genetic Architecture of a Spontaneous Murine Lymphoma to be CharacterizedWenlong Ren, Zhuoqing Fang, Egor Dolzhenko, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 28, 2026
A Murine Database of Structural Variants Identifies A Candidate Gene for a Spontaneous Murine Lymphoma ModelWenlong Ren, Zhuoqing Fang, Egor Dolzhenko, et al.
Biorxiv : the Preprint Server for Biology|March 11, 2024
CTAT-LR-fusion: accurate fusion transcript identification from long and short read isoform sequencing at bulk or single cell resolutionQian Qin, Victoria Popic, Houlin Yu, et al.
Genome Research|March 14, 2025
Accurate fusion transcript identification from long- and short-read isoform sequencing at bulk or single-cell resolutionQian Qin, Victoria Popic, Kirsty Wienand, et al.
Biorxiv : the Preprint Server for Biology|April 3, 2026
Integrating Long-Read Structural Variant Analysis with single-nucleus RNA-seq to Elucidate Gene Expression Effects in DiseaseKwanho Kim, Zechuan Lin, Sean K Simmons, et al.
Nature Biotechnology|June 8, 2023
High-throughput RNA isoform sequencing using programmed cDNA concatenationAziz M Al'Khafaji, Jonathan T Smith, Kiran V Garimella, et al.
Biorxiv : the Preprint Server for Biology|February 23, 2026
Accurate strand-specific long-read transcript isoform discovery and quantification at bulk, single-cell, and single-nucleus resolutionHoulin Yu, Christophe H Georgescu, Akanksha Khorgade, et al.
Pageof 2