Center for non-coding RNA in Technology and Health (RTH)

The center aims at developing technologies, computational methods as well as experimental approaches for analysis of the mammalian genome for non-coding RNAs in relation to (inflammatory) diseases. The center will focus on developing these technologies to exploit them and the findings in relation to diabetes. The center consists of a number of national and international partners, with the core located at the Faculty for Health and Medical Sciences of University of Copenhagen .

The people in the center cover a range of expertises including computational biology, RNA bioinformatics, molecular models in diabetes, RNA biology, animal models, functional genomics and high-throughput sequence analysis..

Join us


We are always looking for motivated and talented young scientists as well as projects or colaborations within the areas of the center. Feel free to contact us with suggestions or to ask for more information.

News

CRISPR Cas9 base editing efficiencies

crispron-be

Excited that the collaboration with Yonglun Luo lab on base editing gRNA design has been published in Nature Communications. We generated efficiency and outcome data for ~20000 gRNAs and employed deep learning learning models trained on ours and publicly available data by labeling the individual data sets resulting in a cutting-edge base editor design tool. See the paper here.

Previous news.

Events


10th Annual Bioinformatics Conference 2026

The Danish Bioinformatics Conference, under the umbrella of ELIXIR Denmark (www.elixir-denmark.org) will start at 12:00 pm on Tuesday, October 27 and end at 16.30 pm on Wednesday, October 28, 2026 at the University of Southern Denmark.

There will be keynote speakers, poster sessions and several parallel in-person workshops.

For more details and registration, please go to the event website to  signup.

Registration deadline: October 4, 2025

Previous events.

Recent resources


TADBpred

Database

Systematical evaluation of the heterogeneity of topologically associating domain boundaries in large genomic context in human

CRISPRon-be

Webserver and Software

Deep learning models simultaneously trained on multiple datasets improve base-editing activity prediction

cyanobacteria CRISPRi

Data Resource

This browsers show the CRISPRi-dCas9 results for a genome-wide knockdown experimental series in Synechocystis sp. PCC 6803 under 4% and 30% CO2 concentrations

Research outset


The human genome, made up of DNA, consists of three billion building blocks (nucleotides) where some regions (stretches) are complete genes. We all carry variants of the genes and some cause diseases. Here, the goal is to investigate the specific class of genes, the non-coding RNA genes, in relation to diabetes. The non-coding RNA (ncRNA) genes can be the missing components in diseases that previously have been overlooked.

Our research goal is to develop technologies for ncRNA analysis and to search for functional ncRNAs in relation to diabetes and other (inflammatory) diseases.

Research in details .

Recent publications


Integrating heterogeneity into topologically associating domain boundary prediction in large genomic context in human

Sun Y, Jensen LJ, Tommerup N, Gorodkin J* NAR Genom Bioinform. 2026 Aug 14;8(3):lqag092. eCollection 2026 Sep
[ PubMed | Paper ]

Systematic evaluation of the heterogeneity of topologically associating domain boundaries in a large genomic context in humans

Sun Y, Tommerup N, Jensen LJ, Gorodkin J* NAR Genom Bioinform. 2026 Aug 14;8(3):lqag093. eCollection 2026 Sep
[ PubMed | Paper ]