Roni Cohen-Fultheim
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Roni Cohen-Fultheim has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Eli Eisenberg
Raymond and Beverly Sackler School of Physics and Astronomy, Tel Aviv University, Tel Aviv, Israel
1 shared publication Erez Y. Levanon
Bar-Ilan University
1 shared publication- Erez Y. Levanon
Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel
1 shared publication - Haim Krupkin
Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat Gan, Israel
1 shared publication - Itamar Twersky
Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat Gan, Israel
1 shared publication - Shalom Hillel Roth
Institute of Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat Gan, Israel
1 shared publication
Latest Publications
- Open Access
- 17 June 2026
- Published by Springer Nature in Genome Biology
- Vol. 27 (1)
A cytoplasmic index for quantifying immune-related A-to-I RNA editing
Distinguishing self from non-self is a major challenge for the immune system. Endogenous cytoplasmic double-stranded RNA (dsRNA) can mimic viral RNA and ac
- 17 June 2026
- Published by Springer Nature in Genome Biology
- Vol. 27 (1)
Open AccessA cytoplasmic index for quantifying immune-related A-to-I RNA editing
Distinguishing self from non-self is a major challenge for the immune system. Endogenous cytoplasmic double-stranded RNA (dsRNA) can mimic viral RNA and ac
- 30 July 2020
- Published by Springer Nature
- Vol. 2181, 213-227
Detection of A-to-I Hyper-edited RNA Sequences
Following A-to-I editing of double-stranded RNA (dsRNA) molecules, sequencing reactions interpret the edited inosine (I) as guanosine (G). For this reason, current methods to detect A-to-I editing sites work to align RNA sequences to their reference DNA sequence in order to reveal A-to-G mismatches. However, areas with heavily edited reads produce dense clusters of A-to-G mismatches that hinder alignment, and complicate correct identification of the sites. The presented approach employs prudent alignment and examination of excessive mismatch events, enabling high-accuracy detection of hyper-edited reads and sites.
- 30 July 2020
- Published by Springer Nature
- Vol. 2181, 213-227
Detection of A-to-I Hyper-edited RNA Sequences
Following A-to-I editing of double-stranded RNA (dsRNA) molecules, sequencing reactions interpret the edited inosine (I) as guanosine (G). For this reason, current methods to detect A-to-I editing sites work to align RNA sequences to their reference DNA sequence in order to reveal A-to-G mismatches. However, areas with heavily edited reads produce dense clusters of A-to-G mismatches that hinder alignment, and complicate correct identification of the sites. The presented approach employs prudent alignment and examination of excessive mismatch events, enabling high-accuracy detection of hyper-edited reads and sites.