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Christian Höner zu Siederdissen

Researcher at Leipzig University

Publications -  45
Citations -  4339

Christian Höner zu Siederdissen is an academic researcher from Leipzig University. The author has contributed to research in topics: RNA & Rfam. The author has an hindex of 14, co-authored 42 publications receiving 3445 citations. Previous affiliations of Christian Höner zu Siederdissen include University of Copenhagen & Max Planck Society.

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ViennaRNA Package 2.0

TL;DR: In this article, exact dynamic programming algorithms can be used to compute ground states, base pairing probabilities, as well as thermodynamic properties of nucleic acids based on carefully measured thermodynamic parameters.
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Next-generation sequencing of the Chinese hamster ovary microRNA transcriptome: Identification, annotation and profiling of microRNAs as targets for cellular engineering

TL;DR: Deep-sequencing small RNA fractions of 6 biotechnologically relevant cell lines and cDNA sequencing of 26 validated targets of miR-17-92 suggests conserved functions for miRNAs in CHO cells, which together with the now publicly available sequence information sets the stage for developing novel RNAi tools for CHO cell engineering.
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Predicting RNA 3D structure using a coarse-grain helix-centered model.

TL;DR: This work proposes that given the wide range of conformational space that needs to be explored, a coarse-grain approach can explore more conformations in less iterations than an all-atom model coupled to a fine-grain energy function.
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A folding algorithm for extended RNA secondary structures

TL;DR: A theoretical model capturing both RNA pair families and extended secondary structure motifs with shared nucleotides using 2-diagrams is presented, accompanying this model with a number of programs for parameter optimization and structure prediction.
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2D Meets 4G: G-Quadruplexes in RNA Secondary Structure Prediction

TL;DR: With preliminary energy parameters, it is found that the overwhelming majority of putative quadruplex-forming sequences in the human genome are likely to fold into canonical secondary structures instead.