Detailed Information on Publication Record
2020
TE-greedy-nester: structure-based detection of LTR retrotransposons and their nesting
LEXA, Matej, Pavel JEDLICKA, Ivan VANÁT, Michal ČERVEŇANSKÝ, Eduard KEJNOVSKÝ et. al.Basic information
Original name
TE-greedy-nester: structure-based detection of LTR retrotransposons and their nesting
Authors
LEXA, Matej (703 Slovakia, guarantor, belonging to the institution), Pavel JEDLICKA (203 Czech Republic), Ivan VANÁT (703 Slovakia, belonging to the institution), Michal ČERVEŇANSKÝ (703 Slovakia, belonging to the institution) and Eduard KEJNOVSKÝ (203 Czech Republic)
Edition
Bioinformatics, OXFORD, OXFORD UNIV PRESS, 2020, 1367-4803
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10201 Computer sciences, information science, bioinformatics
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.937
RIV identification code
RIV/00216224:14330/20:00118965
Organization unit
Faculty of Informatics
UT WoS
000605690100003
Keywords in English
TRANSPOSABLE ELEMENTS; VISUALIZATION; ANNOTATION; IDENTIFICATION; PALEONTOLOGY; PROGRAM; SEARCH; FINDER; TENEST
Tags
International impact, Reviewed
Změněno: 14/5/2021 07:00, RNDr. Pavel Šmerk, Ph.D.
Abstract
V originále
Transposable elements (TEs) in eukaryotes often get inserted into one another, forming sequences that become a complex mixture of full-length elements and their fragments. The reconstruction of full-length elements and the order in which they have been inserted is important for genome and transposon evolution studies. However, the accumulation of mutations and genome rearrangements over evolutionary time makes this process error-prone and decreases the efficiency of software aiming to recover all nested full-length TEs. We created software that uses a greedy recursive algorithm to mine increasingly fragmented copies of full-length LTR retrotransposons in assembled genomes and other sequence data. The software called TE-greedy-nester considers not only sequence similarity but also the structure of elements. This new tool was tested on a set of natural and synthetic sequences and its accuracy was compared to similar software. We found TE-greedy-nester to be superior in a number of parameters, namely computation time and full-length TE recovery in highly nested regions.
Links
GA18-00258S, research and development project |
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