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Monika Krzak

Showing results (1-10 of 7) with videos related to

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Frontiers in Genetics|January 11, 2020
Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering MethodsMonika Krzak, Yordan Raykov, Alexis Boukouvalas, et al.
Briefings in Bioinformatics|July 30, 2021
Demystifying emerging bulk RNA-Seq applications: the application and utility of bioinformatic methodologyAmarinder Singh Thind, Isha Monga, Prasoon Kumar Thakur, et al.
Genome Research|February 24, 2023
The aberrant epigenome of <i>DNMT3B</i>-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memoryVarsha Poondi Krishnan, Barbara Morone, Shir Toubiana, et al.
Nature Communications|August 27, 2025
Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease riskOmar El Garwany, Nikolaos I Panousis, Andrew Knights, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Cell-type-resolved genetic regulatory variation shapes inflammatory bowel disease riskTobi Alegbe, Bradley T Harris, Laura Fachal, et al.
Nature|June 3, 2026
Cell-type-resolved genetic variation shapes inflammatory bowel disease riskTobi Alegbe, Bradley T Harris, Laura Fachal, et al.
Nature Genetics|June 15, 2026
Single-cell RNA sequencing of terminal ileal biopsies identifies signatures of Crohn's disease pathogenesisMonika Krzak, Tobi Alegbe, D Leland Taylor, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Frontiers in Genetics|January 11, 2020
Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering MethodsMonika Krzak, Yordan Raykov, Alexis Boukouvalas, et al.
Briefings in Bioinformatics|July 30, 2021
Demystifying emerging bulk RNA-Seq applications: the application and utility of bioinformatic methodologyAmarinder Singh Thind, Isha Monga, Prasoon Kumar Thakur, et al.
Genome Research|February 24, 2023
The aberrant epigenome of <i>DNMT3B</i>-mutated ICF1 patient iPSCs is amenable to correction, with the exception of a subset of regions with H3K4me3- and/or CTCF-based epigenetic memoryVarsha Poondi Krishnan, Barbara Morone, Shir Toubiana, et al.
Nature Communications|August 27, 2025
Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease riskOmar El Garwany, Nikolaos I Panousis, Andrew Knights, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Cell-type-resolved genetic regulatory variation shapes inflammatory bowel disease riskTobi Alegbe, Bradley T Harris, Laura Fachal, et al.
Nature|June 3, 2026
Cell-type-resolved genetic variation shapes inflammatory bowel disease riskTobi Alegbe, Bradley T Harris, Laura Fachal, et al.
Nature Genetics|June 15, 2026
Single-cell RNA sequencing of terminal ileal biopsies identifies signatures of Crohn's disease pathogenesisMonika Krzak, Tobi Alegbe, D Leland Taylor, et al.
Pageof 1