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Ibrahim Ihsan Taskiran

Showing results (1-10 of 8) with videos related to

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Elife|December 7, 2021
Analysis of long and short enhancers in melanoma cell statesDavid Mauduit, Ibrahim Ihsan Taskiran, Liesbeth Minnoye, et al.
Genome Research|April 9, 2021
Interpretation of allele-specific chromatin accessibility using cell state-aware deep learningZeynep Kalender Atak, Ibrahim Ihsan Taskiran, Jonas Demeulemeester, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 20, 2018
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disabilitySomayeh Kazeminasab, Ibrahim Ihsan Taskiran, Zohreh Fattahi, et al.
Molecular Systems Biology|May 21, 2020
Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomicsCarmen Bravo González-Blas, Xiao-Jiang Quan, Ramon Duran-Romaña, et al.
Nature Cell Biology|January 5, 2024
Single-cell spatial multi-omics and deep learning dissect enhancer-driven gene regulatory networks in liver zonationCarmen Bravo González-Blas, Irina Matetovici, Hanne Hillen, et al.
Genome Research|August 1, 2020
Cross-species analysis of enhancer logic using deep learningLiesbeth Minnoye, Ibrahim Ihsan Taskiran, David Mauduit, et al.
Nature|January 6, 2022
Decoding gene regulation in the fly brainJasper Janssens, Sara Aibar, Ibrahim Ihsan Taskiran, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Elife|December 7, 2021
Analysis of long and short enhancers in melanoma cell statesDavid Mauduit, Ibrahim Ihsan Taskiran, Liesbeth Minnoye, et al.
Genome Research|April 9, 2021
Interpretation of allele-specific chromatin accessibility using cell state-aware deep learningZeynep Kalender Atak, Ibrahim Ihsan Taskiran, Jonas Demeulemeester, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 20, 2018
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disabilitySomayeh Kazeminasab, Ibrahim Ihsan Taskiran, Zohreh Fattahi, et al.
Molecular Systems Biology|May 21, 2020
Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomicsCarmen Bravo González-Blas, Xiao-Jiang Quan, Ramon Duran-Romaña, et al.
Nature Cell Biology|January 5, 2024
Single-cell spatial multi-omics and deep learning dissect enhancer-driven gene regulatory networks in liver zonationCarmen Bravo González-Blas, Irina Matetovici, Hanne Hillen, et al.
Genome Research|August 1, 2020
Cross-species analysis of enhancer logic using deep learningLiesbeth Minnoye, Ibrahim Ihsan Taskiran, David Mauduit, et al.
Nature|January 6, 2022
Decoding gene regulation in the fly brainJasper Janssens, Sara Aibar, Ibrahim Ihsan Taskiran, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Pageof 1