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[[File:{{#setmainimage:Rna.png}}|alt=example image|center|frameless]]
{{Infobox software
| name                = RNA World (beta)
| logo                = Rna.png
| logo caption        = RNA World logo
| screenshot          =
| caption              = RNA World BOINC application screenshot


[https://www.rnaworld.de/rnaworld/ '''''RNA World (beta)'''''] is a '''''[[wikipedia:Volunteer computing|volunteer distributed computing]]''''' project that uses the BOINC platform and needs your help to advance RNA-related research.
| status              = Inactive
| category            = Bioinformatics, Molecular biology, RNA research
| compute              = CPU
| dependencies        = BOINC, VirtualBox (for some applications)


== Why RNA World (beta)? ==
| developer            = Rechenkraft.net e.V.
Every [http://en.wikipedia.org/wiki/Protein protein] in a cell is produced from a transiently synthesized messenger molecule, termed mRNA. This mRNA is then recognized by a cellular machinery that translates the base sequence of mRNA into its corresponding protein (which is a sequence of amino acids). This protein synthesis machinery, termed [http://en.wikipedia.org/wiki/Ribosome ribosome], is actually a [http://en.wikipedia.org/wiki/Ribozyme ribozyme], i.e. it is a catalytically active assembly of several RNA molecules. Consequently, RNAs do not only serve as messenger molecules or perform structural functions as e.g. in [http://en.wikipedia.org/wiki/TRNA tRNA] but may also act as catalysts that perform biochemical reactions as is the case for protein enzymes. Of course, the ribosome also contains numerous proteins as it is a very complex [http://en.wikipedia.org/wiki/Ribonucleoprotein ribonucleoprotein] particle but these predominantly serve structural functions, e.g. to give the ribosome its shape.
| sponsor              = Rechenkraft.net e.V.
| maintainer          = Dr. Michael H. W. Weber and the RNA World team
| released            = {{Start date and age|2010|01|01}}
| repository          = https://www.rnaworld.de/rnaworld/


Fascinatingly, the initial analysis of the human [http://en.wikipedia.org/wiki/Genome genome] sequence revealed that, apparently, only a very small fraction of the [http://en.wikipedia.org/wiki/Dna DNA] of our genome is encoding proteins. Scientists at first thought "''what is all this junk DNA about?''" or "''can't we just delete it?''". Today, it has become clear that probably a major fraction of regulatory events taking place in a human [http://en.wikipedia.org/wiki/Cell_%28biology%29 cell] might be governed by small RNAs, the so-called [http://en.wikipedia.org/wiki/MiRNA miRNAs]. Among other functions, these appear responsible for making sure that a skin cell becomes a skin cell while a muscle, liver or hair [http://en.wikipedia.org/wiki/Cellular_differentiation cell differentiates] to a muscle, liver or hair cell during development and all this although the genetic material (DNA) of all of these very different cell types is essentially identical. On top of that it seems that many cancer types are accompanied by or even result from a deregulated miRNA profile in the affected cell. Moreover, viruses have been discovered to bring along miRNAs to modify the target cell's regulatory network leading to diseases.
| programming language = C, C++, Python
| operating system    = Windows, Linux, macOS
| size                = Variable depending on work unit and VirtualBox image


Hence, it can be clearly stated that RNA research, e.g. by supporting the RNA World distributed supercomputer project, will ultimately lead to important discoveries that might also have significant impact on future health care.
| website              = {{URL|https://www.rnaworld.de/rnaworld/}}
| license              = Open source components and scientific software
}}


== Goal ==
[[File:{{#setmainimage:Rna.png}}|alt=RNA World logo|center|frameless]]
RNA World is a volunteer distributed supercomputer that uses Internet-connected computers to advance RNA research. This system is dedicated to identify, analyze, structurally predict and design RNA molecules on the basis of established bioinformatics software in a high-performance, high-throughput fashion.


In contrast to classical bioinformatic approaches, RNA World does not rely on individual desktop computers, web servers or supercomputers. Instead, it represents a continuously evolving cluster of world-wide distributed machines of any type. As such, RNA World is very heterogenous and, depending on the sub-project, currently addresses Internet-connected computers running Linux, Windows and OSX operating systems - your computer could be an important part of it. The fact that hardware and electricity costs are shared among the volunteer contributors raises the possibility of performing interesting analyses which under economical aspects would often not be affordable. In return, RNA World is not for profit, exclusively uses open source code and will make its results available to the public.
[https://www.rnaworld.de/rnaworld/ '''''RNA World (beta)'''''] is a [[wikipedia:Volunteer computing|volunteer distributed computing]] project based on the [[wikipedia:Berkeley Open Infrastructure for Network Computing|BOINC]] platform. The project is operated by the German non profit organization Rechenkraft.net e.V. and focuses on large scale computational analysis of ribonucleic acid (RNA) molecules and RNA related biological processes.<ref>{{cite web |url=https://www.rnaworld.de/rnaworld/ |title=RNA World |publisher=RNA World |access-date=2026-05-26}}</ref>


In its present form, RNA World runs a fully automated high-throughput analysis software version of Infernal<sup>1</sup>, a program suite originally developed in Sean Eddys laboratory for the systematic identification of non-coding RNAs. The goal of this RNA World sub-project is to systematically identify all known RNA family members in all organisms known to date and make the results available to the public in a timely fashion. With your help, we also aim at supplying established bioinformatic databases such as Rfam<sup>2</sup> with our results to help reduce their future maintenance costs.
RNA World distributes scientific calculations to Internet connected volunteer computers around the world. Participants donate unused CPU processing time to help researchers identify, analyze, classify, and model biologically important RNA structures and sequences. The project collaborates with academic institutions including the Philipps University of Marburg and the Indian Institute of Science in Bangalore.<ref>{{cite web |url=https://www.rechenkraft.net/wiki/RNA_World/Project_description/en |title=RNA World Project Description |publisher=Rechenkraft.net Wiki |access-date=2026-05-26}}</ref>


In contrast to other distributed and grid computing projects, the RNA World developers are currently designing generalized user interfaces that, in parallel to the projects our own research team is following up, allow non-associated individual scientists to submit their own projects in a manner similar to using a web server interface - of course, free of cost.[https://www.rechenkraft.net/wiki/RNA_World/Project_description/en]
== Overview ==


Also see [https://www.rechenkraft.net/wiki/RNA_World/Scientific_objectives scientific objectives here].
RNA molecules perform a wide range of biological functions beyond their traditional role as intermediaries between DNA and proteins. Modern molecular biology has shown that RNA molecules can act as enzymes, regulators, structural elements, and signaling molecules. One of the most notable examples is the ribosome, a complex ribonucleoprotein assembly responsible for protein synthesis. The catalytic core of the ribosome is itself composed primarily of RNA, making it a natural ribozyme.<ref>{{cite journal
|last1=Steitz
|first1=Thomas A.
|title=A structural understanding of the dynamic ribosome machine
|journal=Nature Reviews Molecular Cell Biology
|year=2008
|volume=9
|issue=3
|pages=242–253
|doi=10.1038/nrm2352
}}</ref>


== Methods ==
The project takes its name from the [[wikipedia:RNA world|RNA world hypothesis]], a scientific theory proposing that early life on Earth may have relied primarily on RNA molecules before the evolution of DNA and proteins. In this model, RNA would have served both as genetic material and as a catalytic molecule capable of supporting primitive biochemical reactions.<ref>{{cite journal
|last1=Gilbert
|first1=Walter
|title=The RNA World
|journal=Nature
|year=1986
|volume=319
|issue=6055
|pages=618
|doi=10.1038/319618a0
}}</ref>


==== Important information for users with VirtualBox installed ====
Many RNA molecules fold into complex secondary and tertiary structures governed by base pairing interactions. RNA folding predictions frequently involve thermodynamic calculations that minimize free energy. Typical RNA folding algorithms attempt to minimize:
If you have VirtualBox installed on your computer and participate in this project please note:


* in order to get tasks your CPU needs to have virtualisation capabilities (AMD-v or VT-x)
<math>\Delta G = \Delta H - T\Delta S</math>
* those virtualisation capabilities need to be '''enabled''' in your BIOS settings or all tasks will error out
* Some tasks are '''incompatible with newer VirtualBox versions''': If you have 1.15 or earlier tasks, you must use VirtualBox 4.3.x or earlier. If you have 1.17 tasks, you must use VirtualBox 5.0.x or earlier. If you have 1.18 tasks, you may use VirtualBox 5.1.x. If you have 1.19 tasks, you may use VirtualBox 5.2.x.
* a BOINC client of at least 7.2.33 is recommended
* The runtime of the cmsearch VM apps are very long '''(>1000 hours)''' and deadlines are automatically extended but only visible on the website!


== Project team / Sponsors ==
where <math>\Delta G</math> is the Gibbs free energy of folding, <math>\Delta H</math> is enthalpy, <math>T</math> is temperature, and <math>\Delta S</math> is entropy.<ref>{{cite journal
This project was created within the [https://www.rechenkraft.net/wiki/Rechenkraft.net_e.V. Apothekerkraft.net eV association] and is operated exclusively by volunteers. The cooperation partners are the Philipps University of Marburg and the Indian Institute of Science in Bangalore (India).
|last1=Mathews
RNA World is run byrechner.net eV in Germany.
|first1=David H.
|title=Revolutions in RNA secondary structure prediction
|journal=Journal of Molecular Biology
|year=2006
|volume=359
|issue=3
|pages=526–532
|doi=10.1016/j.jmb.2006.01.067
}}</ref>
 
== Scientific background ==
 
Every protein in a living cell is synthesized from a messenger RNA molecule, commonly abbreviated as mRNA. During translation, ribosomes decode the nucleotide sequence of mRNA into a corresponding amino acid sequence. RNA molecules are therefore central to nearly all known biological systems.
 
The sequencing of the human genome revealed that only a relatively small portion of human DNA directly encodes proteins. Subsequent research demonstrated that large regions of the genome produce non coding RNAs involved in regulation, cellular differentiation, and gene expression. Among the most important classes are microRNAs (miRNAs), short RNA molecules that regulate messenger RNA stability and translation.<ref>{{cite journal
|last1=Bartel
|first1=David P.
|title=MicroRNAs: genomics, biogenesis, mechanism, and function
|journal=Cell
|year=2004
|volume=116
|issue=2
|pages=281–297
|doi=10.1016/S0092-8674(04)00045-5
}}</ref>
 
MicroRNAs are now known to play important roles in development, cancer biology, viral infection, and cellular differentiation. Misregulation of miRNA expression has been associated with many diseases including leukemia, breast cancer, and neurological disorders.<ref>{{cite journal
|last1=Calin
|first1=George A.
|last2=Croce
|first2=Carlo M.
|title=MicroRNA signatures in human cancers
|journal=Nature Reviews Cancer
|year=2006
|volume=6
|issue=11
|pages=857–866
|doi=10.1038/nrc1997
}}</ref>
 
== Goals ==
 
RNA World was designed as a distributed bioinformatics platform capable of performing large scale RNA analysis using volunteer computing resources contributed by the public. Unlike conventional centralized supercomputers, the project operates as a heterogeneous distributed cluster composed of thousands of independently managed computers across multiple operating systems and hardware configurations.<ref>{{cite web
|url=https://www.rechenkraft.net/wiki/RNA_World/Scientific_objectives
|title=RNA World Scientific Objectives
|publisher=Rechenkraft.net Wiki
|access-date=2026-05-26
}}</ref>
 
The project aims to:
 
* identify novel non coding RNA molecules
* analyze RNA sequence conservation across species
* predict RNA secondary structures
* support comparative genomics studies
* contribute results to established RNA databases such as [[wikipedia:Rfam|Rfam]]
* provide computational resources for RNA related scientific investigations
 
One major RNA World application uses the Infernal software suite, originally developed in the laboratory of Sean Eddy. Infernal uses covariance models to identify homologous RNA sequences and conserved secondary structures in genomic datasets.<ref>{{cite journal
|last1=Nawrocki
|first1=Eric P.
|last2=Eddy
|first2=Sean R.
|title=Infernal 1.1: 100 fold faster RNA homology searches
|journal=Bioinformatics
|year=2013
|volume=29
|issue=22
|pages=2933–2935
|doi=10.1093/bioinformatics/btt509
}}</ref>
 
Covariance models combine sequence conservation and structural conservation into probabilistic scoring systems. The probability of a sequence alignment may be represented by:
 
<math>P(S,M) = \prod_i P(s_i \mid m_i)</math>
 
where <math>S</math> represents the observed sequence and <math>M</math> represents the covariance model state path.
 
== Volunteer computing ==
[[File:BOINC Manager Screenshot.jpg|thumb|467x467px|BOINC Manager software used to connect to RNA World]]
RNA World uses the BOINC middleware platform developed at the [[wikipedia:University of California, Berkeley|University of California, Berkeley]]. BOINC enables scientific projects to distribute computational workloads to volunteer computers connected through the Internet.<ref>{{cite journal
|last1=Anderson
|first1=David P.
|title=BOINC: A System for Public Resource Computing and Storage
|journal=Proceedings of the Fifth IEEE/ACM International Workshop on Grid Computing
|year=2004
|doi=10.1109/GRID.2004.14
}}</ref>
 
Participants install the BOINC client software and attach their computers to RNA World. Work units are downloaded automatically, processed locally, and returned to the project servers upon completion.
 
The project has historically supported Linux, Microsoft Windows, and macOS systems. Some applications additionally require [[wikipedia:Oracle VM VirtualBox|VirtualBox]] virtualization support.
 
== VirtualBox applications ==
 
Several RNA World applications operate within virtualized environments using VirtualBox. These applications allow researchers to deploy complex Linux based bioinformatics pipelines independent of the volunteer's host operating system.
 
Users participating in VirtualBox based applications must ensure that hardware virtualization extensions such as AMD V or Intel VT x are enabled in the system BIOS or UEFI firmware. Older RNA World applications also depended on specific VirtualBox versions for compatibility.
 
Some cmsearch virtual machine tasks are known for extremely long runtimes exceeding 1000 hours. Deadlines may be automatically extended by the project server.<ref>{{cite web
|url=https://www.rechenkraft.net/wiki/RNA_World/Project_description/en
|title=RNA World Project Description
|publisher=Rechenkraft.net Wiki
|access-date=2026-05-26
}}</ref>
 
== Project organization ==
 
RNA World was created within the Rechenkraft.net e.V. volunteer computing community and is operated entirely by volunteers. The project infrastructure, software maintenance, and scientific administration are maintained collaboratively.
 
=== Active development team ===


==== RNA World Personal (active development team) ====
{| class="wikitable"
{| class="wikitable"
|project Manager
! Role
|[https://www.rechenkraft.net/wiki/Benutzer:Michael_H.W._Weber Dr. Michael HW Weber]
! Staff
|-
|-
|Server administrator
| Project manager
|Christian Beer & Uwe Beckert ( [https://www.rechenkraft.net/wiki/Benutzer:Yoyo Yoyo] )
| Dr. Michael H. W. Weber
|-
|-
|Software development
| Server administration
|Christian Beer, Tilman Giese (coturnix), Volker Hatzenberger (Ananas), Nico Mittenzwey (Nico), Stephan Ude (Mueslirocker)
| Christian Beer and Uwe Beckert
|-
|-
|Graphics & Design
| Software development
|Lasse J. Kolb, Rebirther, Dr. Michael HW Weber
| Christian Beer, Tilman Giese, Volker Hatzenberger, Nico Mittenzwey, Stephan Ude
|-
|-
|e-mail
| Graphics and design
|mw @ rnaworld.de
| Lasse J. Kolb, Rebirther, Dr. Michael H. W. Weber
|}
|}


==== RNA World Staff (former members) ====
=== Former contributors ===


* Martin (Linuxfan) Bertheau: BOINC progress bar, Linux checkpointing
{| class="wikitable"
* Jacques Kühl: General checkpointing mechanism
! Contributor
* Maximilian (mxplm) Palm: Development of the "job submission" interface for end users
! Contribution
* Andre Schmitz (Grodahn): ARM software development
|-
| Martin Bertheau
| Linux checkpointing and BOINC progress bar improvements
|-
| Jacques Kühl
| General checkpointing mechanisms
|-
| Maximilian Palm
| Development of the user job submission interface
|-
| Andre Schmitz
| ARM software development
|}


== Scientific publications ==
== Scientific publications ==


# Hoch, Philipp G., Olga Y. Burenina, Michael H.W. Weber, Daria A. Elkina, Mikhail V. Nesterchuk, Petr V. Sergiev, Roland K. Hartmann and Elena A. Kubareva. [https://linkinghub.elsevier.com/retrieve/pii/S0300908415000024 Phenotypic characterization and complementation analysis of Bacillus subtilis 6S RNA single and double deletion mutants]. Biochimie (2015). DOI: 10.1016/j.biochi.2014.12.019.
Research associated with RNA World has contributed to multiple peer reviewed publications in molecular biology, RNA biochemistry, and ribosome research.
# Sinha, Akesh, Caroline Köhrer, Michael H.W. Weber, Isao Masuda, Vamsi K. Mootha, Ya-Ming Hou and Uttam L. RajBhandary. [https://linkinghub.elsevier.com/retrieve/pii/S0021925820474757 Biochemical Characterization of Pathogenic Mutations in Human Mitochondrial Methionyl-tRNA Formyltransferase]. Journal of Biological Chemistry (2014). DOI: 10.1074/jbc.M114.610626.
 
# Arora, Smriti, Satya Prathyusha Bhamidimarri, Michael H. W. Weber and Umesh Varshney. [https://journals.asm.org/doi/10.1128/JB.00455-13 Role of the Ribosomal P-Site Elements of m 2 G966, m 5 C967, and the S9 C-Terminal Tail in Maintenance of the Reading Frame during Translational Elongation in Escherichia coli]. Journal of Bacteriology (2013). DOI: 10.1128/JB.00455-13.
# Hoch, Philipp G. ''et al.'' "Phenotypic characterization and complementation analysis of ''Bacillus subtilis'' 6S RNA single and double deletion mutants." ''Biochimie'' (2015). DOI: 10.1016/j.biochi.2014.12.019.
# Arora, S., S. P. Bhamidimarri, M. Bhattacharyya, A. Govindan, M. H. W. Weber, S. Vishveshwara and U. Varshney. [https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gkt175 Distinctive contributions of the ribosomal P-site elements m2G966, m5C967 and the C-terminal tail of the S9 protein in the fidelity of initiation of translation in Escherichia coli]. Nucleic Acids Research (2013). DOI: 10.1093/nar/gkt175.
# Sinha, Akesh ''et al.'' "Biochemical Characterization of Pathogenic Mutations in Human Mitochondrial Methionyl tRNA Formyltransferase." ''Journal of Biological Chemistry'' (2014). DOI: 10.1074/jbc.M114.610626.
# Seshadri, Anuradha, Badrinath Dubey, Michael H. W. Weber and Umesh Varshney. [https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2958.2009.06685.x Impact of rRNA methylations on ribosome recycling and fidelity of initiation in ''Escherichia coli''. Molecular Microbiology (2009)]. DOI: 10.1111/j.1365-2958.2009.06685.x.
# Arora, Smriti ''et al.'' "Role of the Ribosomal P Site Elements of m2G966, m5C967, and the S9 C Terminal Tail in Maintenance of the Reading Frame during Translational Elongation in ''Escherichia coli''." ''Journal of Bacteriology'' (2013). DOI: 10.1128/JB.00455-13.
# Arora, Smriti ''et al.'' "Distinctive contributions of the ribosomal P site elements m2G966, m5C967 and the C terminal tail of the S9 protein in the fidelity of initiation of translation in ''Escherichia coli''." ''Nucleic Acids Research'' (2013). DOI: 10.1093/nar/gkt175.
# Seshadri, Anuradha ''et al.'' "Impact of rRNA methylations on ribosome recycling and fidelity of initiation in ''Escherichia coli''." ''Molecular Microbiology'' (2009). DOI: 10.1111/j.1365-2958.2009.06685.x.
 
== See also ==
 
* [[wikipedia:BOINC|BOINC]]
* [[wikipedia:RNA world|RNA world hypothesis]]
* [[wikipedia:Bioinformatics|Bioinformatics]]
* [[wikipedia:Rfam|Rfam]]
* [[wikipedia:Infernal (software)|Infernal]]
* [[wikipedia:Volunteer computing|Volunteer computing]]
 
== External links ==
 
* [https://www.rnaworld.de/rnaworld/ Official RNA World website]
* [https://www.rechenkraft.net/wiki/RNA_World/Project_description/en RNA World project description]
* [https://www.rechenkraft.net/ Rechenkraft.net e.V.]
* [https://boinc.berkeley.edu/ BOINC]
 
== References ==
 
{{Reflist}}

Revision as of 12:42, 26 May 2026







RNA World (beta)
Project
StatusInactive
CategoryBioinformatics, Molecular biology, RNA research
ComputeCPU
RequiresBOINC, VirtualBox (for some applications)
Development
DeveloperRechenkraft.net e.V.
SponsorRechenkraft.net e.V.
MaintainerDr. Michael H. W. Weber and the RNA World team
Initial releaseJanuary 1, 2010  (16 years ago)
Repositoryhttps://www.rnaworld.de/rnaworld/
Software
Written inC, C++, Python
Operating systemWindows, Linux, macOS
SizeVariable depending on work unit and VirtualBox image
Metadata
Websitehttps://www.rnaworld.de/rnaworld/
LicenseOpen source components and scientific software

[[File:{{#setmainimage:Rna.png}}|alt=RNA World logo|center|frameless]]

RNA World (beta) is a volunteer distributed computing project based on the BOINC platform. The project is operated by the German non profit organization Rechenkraft.net e.V. and focuses on large scale computational analysis of ribonucleic acid (RNA) molecules and RNA related biological processes.[1]

RNA World distributes scientific calculations to Internet connected volunteer computers around the world. Participants donate unused CPU processing time to help researchers identify, analyze, classify, and model biologically important RNA structures and sequences. The project collaborates with academic institutions including the Philipps University of Marburg and the Indian Institute of Science in Bangalore.[2]

Overview

RNA molecules perform a wide range of biological functions beyond their traditional role as intermediaries between DNA and proteins. Modern molecular biology has shown that RNA molecules can act as enzymes, regulators, structural elements, and signaling molecules. One of the most notable examples is the ribosome, a complex ribonucleoprotein assembly responsible for protein synthesis. The catalytic core of the ribosome is itself composed primarily of RNA, making it a natural ribozyme.[3]

The project takes its name from the RNA world hypothesis, a scientific theory proposing that early life on Earth may have relied primarily on RNA molecules before the evolution of DNA and proteins. In this model, RNA would have served both as genetic material and as a catalytic molecule capable of supporting primitive biochemical reactions.[4]

Many RNA molecules fold into complex secondary and tertiary structures governed by base pairing interactions. RNA folding predictions frequently involve thermodynamic calculations that minimize free energy. Typical RNA folding algorithms attempt to minimize:

ΔG=ΔHTΔS

where ΔG is the Gibbs free energy of folding, ΔH is enthalpy, T is temperature, and ΔS is entropy.[5]

Scientific background

Every protein in a living cell is synthesized from a messenger RNA molecule, commonly abbreviated as mRNA. During translation, ribosomes decode the nucleotide sequence of mRNA into a corresponding amino acid sequence. RNA molecules are therefore central to nearly all known biological systems.

The sequencing of the human genome revealed that only a relatively small portion of human DNA directly encodes proteins. Subsequent research demonstrated that large regions of the genome produce non coding RNAs involved in regulation, cellular differentiation, and gene expression. Among the most important classes are microRNAs (miRNAs), short RNA molecules that regulate messenger RNA stability and translation.[6]

MicroRNAs are now known to play important roles in development, cancer biology, viral infection, and cellular differentiation. Misregulation of miRNA expression has been associated with many diseases including leukemia, breast cancer, and neurological disorders.[7]

Goals

RNA World was designed as a distributed bioinformatics platform capable of performing large scale RNA analysis using volunteer computing resources contributed by the public. Unlike conventional centralized supercomputers, the project operates as a heterogeneous distributed cluster composed of thousands of independently managed computers across multiple operating systems and hardware configurations.[8]

The project aims to:

  • identify novel non coding RNA molecules
  • analyze RNA sequence conservation across species
  • predict RNA secondary structures
  • support comparative genomics studies
  • contribute results to established RNA databases such as Rfam
  • provide computational resources for RNA related scientific investigations

One major RNA World application uses the Infernal software suite, originally developed in the laboratory of Sean Eddy. Infernal uses covariance models to identify homologous RNA sequences and conserved secondary structures in genomic datasets.[9]

Covariance models combine sequence conservation and structural conservation into probabilistic scoring systems. The probability of a sequence alignment may be represented by:

P(S,M)=iP(simi)

where S represents the observed sequence and M represents the covariance model state path.

Volunteer computing

BOINC Manager software used to connect to RNA World

RNA World uses the BOINC middleware platform developed at the University of California, Berkeley. BOINC enables scientific projects to distribute computational workloads to volunteer computers connected through the Internet.[10]

Participants install the BOINC client software and attach their computers to RNA World. Work units are downloaded automatically, processed locally, and returned to the project servers upon completion.

The project has historically supported Linux, Microsoft Windows, and macOS systems. Some applications additionally require VirtualBox virtualization support.

VirtualBox applications

Several RNA World applications operate within virtualized environments using VirtualBox. These applications allow researchers to deploy complex Linux based bioinformatics pipelines independent of the volunteer's host operating system.

Users participating in VirtualBox based applications must ensure that hardware virtualization extensions such as AMD V or Intel VT x are enabled in the system BIOS or UEFI firmware. Older RNA World applications also depended on specific VirtualBox versions for compatibility.

Some cmsearch virtual machine tasks are known for extremely long runtimes exceeding 1000 hours. Deadlines may be automatically extended by the project server.[11]

Project organization

RNA World was created within the Rechenkraft.net e.V. volunteer computing community and is operated entirely by volunteers. The project infrastructure, software maintenance, and scientific administration are maintained collaboratively.

Active development team

Role Staff
Project manager Dr. Michael H. W. Weber
Server administration Christian Beer and Uwe Beckert
Software development Christian Beer, Tilman Giese, Volker Hatzenberger, Nico Mittenzwey, Stephan Ude
Graphics and design Lasse J. Kolb, Rebirther, Dr. Michael H. W. Weber

Former contributors

Contributor Contribution
Martin Bertheau Linux checkpointing and BOINC progress bar improvements
Jacques Kühl General checkpointing mechanisms
Maximilian Palm Development of the user job submission interface
Andre Schmitz ARM software development

Scientific publications

Research associated with RNA World has contributed to multiple peer reviewed publications in molecular biology, RNA biochemistry, and ribosome research.

  1. Hoch, Philipp G. et al. "Phenotypic characterization and complementation analysis of Bacillus subtilis 6S RNA single and double deletion mutants." Biochimie (2015). DOI: 10.1016/j.biochi.2014.12.019.
  2. Sinha, Akesh et al. "Biochemical Characterization of Pathogenic Mutations in Human Mitochondrial Methionyl tRNA Formyltransferase." Journal of Biological Chemistry (2014). DOI: 10.1074/jbc.M114.610626.
  3. Arora, Smriti et al. "Role of the Ribosomal P Site Elements of m2G966, m5C967, and the S9 C Terminal Tail in Maintenance of the Reading Frame during Translational Elongation in Escherichia coli." Journal of Bacteriology (2013). DOI: 10.1128/JB.00455-13.
  4. Arora, Smriti et al. "Distinctive contributions of the ribosomal P site elements m2G966, m5C967 and the C terminal tail of the S9 protein in the fidelity of initiation of translation in Escherichia coli." Nucleic Acids Research (2013). DOI: 10.1093/nar/gkt175.
  5. Seshadri, Anuradha et al. "Impact of rRNA methylations on ribosome recycling and fidelity of initiation in Escherichia coli." Molecular Microbiology (2009). DOI: 10.1111/j.1365-2958.2009.06685.x.

See also

External links

References

  1. RNA World. RNA World. Retrieved 2026-05-26}.
  2. RNA World Project Description. Rechenkraft.net Wiki. Retrieved 2026-05-26}.
  3. (2008}).A structural understanding of the dynamic ribosome machine. Nature Reviews Molecular Cell Biology. pp. 242–253. DOI: 10.1038/nrm2352.
  4. (1986}).The RNA World. Nature. pp. 618. DOI: 10.1038/319618a0.
  5. (2006}).Revolutions in RNA secondary structure prediction. Journal of Molecular Biology. pp. 526–532. DOI: 10.1016/j.jmb.2006.01.067.
  6. (2004}).MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. pp. 281–297. DOI: 10.1016/S0092-8674(04)00045-5.
  7. (2006}).MicroRNA signatures in human cancers. Nature Reviews Cancer. pp. 857–866. DOI: 10.1038/nrc1997.
  8. RNA World Scientific Objectives. Rechenkraft.net Wiki. Retrieved 2026-05-26}.
  9. (2013}).Infernal 1.1: 100 fold faster RNA homology searches. Bioinformatics. pp. 2933–2935. DOI: 10.1093/bioinformatics/btt509.
  10. (2004}).BOINC: A System for Public Resource Computing and Storage. Proceedings of the Fifth IEEE/ACM International Workshop on Grid Computing. DOI: 10.1109/GRID.2004.14.
  11. RNA World Project Description. Rechenkraft.net Wiki. Retrieved 2026-05-26}.