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Related Concept Videos

MicroRNAs01:22

MicroRNAs

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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns—non-coding regions of a gene—or intergenic regions—stretches of DNA present between genes. Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After...
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MicroRNAs01:22

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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
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HumiR: Web Services, Tools and Databases for Exploring Human microRNA Data.

Jeffrey Solomon1, Fabian Kern1, Tobias Fehlmann1

  • 1Chair for Clinical Bioinformatics, Saarland University, 66123 Saarbrücken, Germany.

Biomolecules
|November 25, 2020
PubMed
Summary
This summary is machine-generated.

HumiR offers a unified web platform for human small non-coding RNA research tools. This resource aids researchers in selecting appropriate tools for tasks like microRNA analysis and expression profiling.

Keywords:
bioinformaticsmicroRNAsnon-coding RNAweb servers

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Area of Science:

  • Bioinformatics
  • Genomics
  • Molecular Biology

Background:

  • Computational tools and databases are crucial for small non-coding RNA research, including microRNAs (miRNAs), piwi-interacting RNAs (piRNAs), and circular RNAs (circRNAs).
  • Existing tools often focus on species-independent analyses, yet a consolidated resource for human-specific small non-coding RNAs is lacking.
  • Interoperability between various tools for miRNA analysis, target prediction, and expression profiling remains a challenge.

Purpose of the Study:

  • To present HumiR, a unified web presence integrating tools for human small non-coding RNA research.
  • To facilitate the selection of appropriate computational tools for diverse miRNA-related research tasks.
  • To establish a foundational step towards a comprehensive knowledge base for human small non-coding RNA research.

Main Methods:

  • Development and integration of human-specific tools for miRNA analysis, including quantification and prediction.
  • Compilation of databases for human miRNAs, their variations, and expression profiles across different tissues and cell types.
  • Creation of helper tools for common tasks like naming conversion and reporter assay design.

Main Results:

  • HumiR provides a centralized access point for a suite of human small non-coding RNA analysis tools.
  • The platform supports tasks such as miRNA quantification, isomiR prediction, target analysis, and expression profiling.
  • Demonstrated utility through a comprehensive analysis of Alzheimer's disease-associated miRNAs.

Conclusions:

  • HumiR enhances accessibility and usability for researchers in the human small non-coding RNA field.
  • The integrated platform streamlines workflows and aids in tool selection for specific research questions.
  • HumiR represents a significant advancement towards a unified knowledge base for human small non-coding RNA research.