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      Characterization, biogenesis model, and current bioinformatics of human extrachromosomal circular DNA

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          Abstract

          Human extrachromosomal circular DNA, or eccDNA, has been the topic of extensive investigation in the last decade due to its prominent regulatory role in the development of disorders including cancer. With the rapid advancement of experimental, sequencing and computational technology, millions of eccDNA records are now accessible. Unfortunately, the literature and databases only provide snippets of this information, preventing us from fully understanding eccDNAs. Researchers frequently struggle with the process of selecting algorithms and tools to examine eccDNAs of interest. To explain the underlying formation mechanisms of the five basic classes of eccDNAs, we categorized their characteristics and functions and summarized eight biogenesis theories. Most significantly, we created a clear procedure to help in the selection of suitable techniques and tools and thoroughly examined the most recent experimental and bioinformatics methodologies and data resources for identifying, measuring and analyzing eccDNA sequences. In conclusion, we highlighted the current obstacles and prospective paths for eccDNA research, specifically discussing their probable uses in molecular diagnostics and clinical prediction, with an emphasis on the potential contribution of novel computational strategies.

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          Most cited references129

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          The Sequence Alignment/Map format and SAMtools

          Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms. It is flexible in style, compact in size, efficient in random access and is the format in which alignments from the 1000 Genomes Project are released. SAMtools implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments. Availability: http://samtools.sourceforge.net Contact: rd@sanger.ac.uk
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            BEDTools: a flexible suite of utilities for comparing genomic features

            Motivation: Testing for correlations between different sets of genomic features is a fundamental task in genomics research. However, searching for overlaps between features with existing web-based methods is complicated by the massive datasets that are routinely produced with current sequencing technologies. Fast and flexible tools are therefore required to ask complex questions of these data in an efficient manner. Results: This article introduces a new software suite for the comparison, manipulation and annotation of genomic features in Browser Extensible Data (BED) and General Feature Format (GFF) format. BEDTools also supports the comparison of sequence alignments in BAM format to both BED and GFF features. The tools are extremely efficient and allow the user to compare large datasets (e.g. next-generation sequencing data) with both public and custom genome annotation tracks. BEDTools can be combined with one another as well as with standard UNIX commands, thus facilitating routine genomics tasks as well as pipelines that can quickly answer intricate questions of large genomic datasets. Availability and implementation: BEDTools was written in C++. Source code and a comprehensive user manual are freely available at http://code.google.com/p/bedtools Contact: aaronquinlan@gmail.com; imh4y@virginia.edu Supplementary information: Supplementary data are available at Bioinformatics online.
              • Record: found
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              SciPy 1.0: fundamental algorithms for scientific computing in Python

              SciPy is an open-source scientific computing library for the Python programming language. Since its initial release in 2001, SciPy has become a de facto standard for leveraging scientific algorithms in Python, with over 600 unique code contributors, thousands of dependent packages, over 100,000 dependent repositories and millions of downloads per year. In this work, we provide an overview of the capabilities and development practices of SciPy 1.0 and highlight some recent technical developments.

                Author and article information

                Contributors
                Role: Role: Role: Role: Role: Role:
                Role: Role: Role:
                Role: Role:
                URI : https://loop.frontiersin.org/people/568269/overviewRole: Role: Role: Role: Role:
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                29 April 2024
                2024
                : 15
                : 1385150
                Affiliations
                [1] 1 School of Medicine , Chongqing University , Department of Clinical Data Research , Chongqing Emergency Medical Center , Chongqing University Central Hospital , Chongqing University , Chongqing, China
                [2] 2 School of Medicine , Jinan University , Guangzhou, Guangdong, China
                Author notes

                Edited by: Eveline M. Ibeagha-Awemu, Agriculture and Agri-Food Canada (AAFC), Canada

                Reviewed by: Lihe Liu, Sanford Burnham Prebys Medical Discovery Institute, United States

                Fengbiao Mao, Peking University Third Hospital, China

                *Correspondence: Lingyun Zou, zoulingyun@ 123456cqu.edu.cn
                Article
                1385150
                10.3389/fgene.2024.1385150
                11092383
                38746056
                6854ab11-9af0-4bd6-b034-e09df328ba23
                Copyright © 2024 Zhou, Tang, Ye and Zou.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 12 February 2024
                : 12 April 2024
                Funding
                Funded by: Science-Health Joint Medical Scientific Research Project of Chongqing , doi 10.13039/100017501;
                Funded by: Natural Science Foundation of Chongqing Municipality , doi 10.13039/501100005230;
                Funded by: Chongqing Municipal Education Commission Foundation , doi 10.13039/100012494;
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This study was supported by the Chongqing medical scientific research project (Joint project of Chongqing Health Commission and Science and Technology Bureau, 2024ZDXM011), the Natural Science Foundation of Chongqing (CSTB2023NSCQ-MSX0237), and the Science and Technology Research Project of Chongqing Municipal Education Commission (KJZD-K202300101).
                Categories
                Genetics
                Systematic Review
                Custom metadata
                Cancer Genetics and Oncogenomics

                Genetics
                extrachromosomal circular dna,biogenesis model,high-throughput sequencing,bioinformatics pipelines,computational tools

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