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Journal of Biomedical Informatics
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October 5, 2023
MAGNETO: Cell type marker panel generator from single-cell transcriptomic data
Andrea Tangherloni, Simone G Riva, Brynelle Myers, et al.
Journal of Visualized Experiments : Jove
|
October 9, 2023
CATCH-UP: A High-Throughput Upstream-Pipeline for Bulk ATAC-Seq and ChIP-Seq Data
Simone G Riva, Emily Georgiades, E Ravza Gur, et al.
Bioinformatics Advances
|
April 7, 2026
Deciphering <i>cis</i>-regulatory elements using REgulamentary
Simone G Riva, Edward Sanders, Emily Georgiades, et al.
Scientific Reports
|
April 6, 2025
Active regulatory elements recruit cohesin to establish cell specific chromatin domains
Emily Georgiades, Caroline Harrold, Nigel Roberts, et al.
Cell Stem Cell
|
May 5, 2023
GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells
Sven Turkalj, Niels Asger Jakobsen, Angus Groom, et al.
Genome Medicine
|
November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Alistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Journal of Biomedical Informatics
|
October 5, 2023
MAGNETO: Cell type marker panel generator from single-cell transcriptomic data
Andrea Tangherloni, Simone G Riva, Brynelle Myers, et al.
Journal of Visualized Experiments : Jove
|
October 9, 2023
CATCH-UP: A High-Throughput Upstream-Pipeline for Bulk ATAC-Seq and ChIP-Seq Data
Simone G Riva, Emily Georgiades, E Ravza Gur, et al.
Bioinformatics Advances
|
April 7, 2026
Deciphering <i>cis</i>-regulatory elements using REgulamentary
Simone G Riva, Edward Sanders, Emily Georgiades, et al.
Scientific Reports
|
April 6, 2025
Active regulatory elements recruit cohesin to establish cell specific chromatin domains
Emily Georgiades, Caroline Harrold, Nigel Roberts, et al.
Cell Stem Cell
|
May 5, 2023
GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells
Sven Turkalj, Niels Asger Jakobsen, Angus Groom, et al.
Genome Medicine
|
November 10, 2023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Alistair T Pagnamenta, Carme Camps, Edoardo Giacopuzzi, et al.
Page
of 1