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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Identification of neoplasm-specific signatures of miRNA interactions by employing a systems biology approach

Thumbnail
Συγγραφέας
Bonab R.A., Asfa S., Kontou P., Karakülah G., Pavlopoulou A.
Ημερομηνία
2022
Γλώσσα
en
DOI
10.7717/peerj.14149
Λέξη-κλειδί
microRNA
microrna 1296 3p
microrna 3689
microrna 3689c
microrna 3689e
microrna 4273
microrna 4422
microrna 4432
microrna 4445 3p
microrna 4694 3p
microrna 4720
microrna 5002
microrna 5002 3p
microrna 5011 3p
microrna 522 2p
microrna 548ae 5p
microrna 548al
microrna 548ao 5p
microrna 5688
microrna 5699
microrna 5699 5p
microrna 5702
microrna 6511b 5p
microrna 6719 3p
microrna 6724 5p
microrna 6748 5p
microrna 6753 3p
microrna 6770 5p
microrna 6773 5p
microrna 6811 5p
microrna 6828 3p
microrna 7107 3p
microrna 7154 5p
microrna 7515
microrna 8062
microrna 8067
microrna 8068
small untranslated RNA
unclassified drug
adenoid cystic carcinoma
Article
bioinformatics
bladder cancer
brain cancer
cancer prognosis
colorectal cancer
epigenome
gene ontology
head and neck cancer
human
lung adenocarcinoma
lung cancer
neoplasm
network analysis
nomenclature
ovary cancer
protein localization
protein RNA binding
skin cancer
squamous cell carcinoma
stomach tumor
systems biology
testis tumor
thyroid follicular carcinoma
PeerJ Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
MicroRNAs represent major regulatory components of the disease epigenome and they constitute powerful biomarkers for the accurate diagnosis and prognosis of various diseases, including cancers. The advent of high-throughput technologies facilitated the generation of a vast amount of miRNA-cancer association data. Computational approaches have been utilized widely to effectively analyze and interpret these data towards the identification of miRNA signatures for diverse types of cancers. Herein, a novel computational workflow was applied to discover core sets of miRNA interactions for the major groups of neoplastic diseases by employing network-based methods. To this end, miRNA-cancer association data from four comprehensive publicly available resources were utilized for constructing miRNA-centered networks for each major group of neoplasms. The corresponding miRNA-miRNA interactions were inferred based on shared functionally related target genes. The topological attributes of the generated networks were investigated in order to detect clusters of highly interconnected miRNAs that form core modules in each network. Those modules that exhibited the highest degree of mutual exclusivity were selected from each graph. In this way, neoplasm-specific miRNA modules were identified that could represent potential signatures for the corresponding diseases. Copyright 2022 Arshinchi Bonab et al.
URI
http://hdl.handle.net/11615/71808
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19674]

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EnglishΕλληνικά
Η δικτυακή πύλη της Ευρωπαϊκής Ένωσης
Ψηφιακή Ελλάδα
ΕΣΠΑ 2007-2013
Με τη συγχρηματοδότηση της Ελλάδας και της Ευρωπαϊκής Ένωσης
htmlmap