RetroSnake: A modular pipeline to detect human endogenous retroviruses in genome sequencing data.
RetroSnake: A modular pipeline to detect human endogenous retroviruses in genome sequencing data.
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DOI:
10.1016/j.isci.2022.105289
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发表时间:
2022-11-18
期刊:
影响因子:
5.8
通讯作者:
Iacoangeli, Alfredo
中科院分区:
文献类型:
--
作者:
Kabiljo, Renata;Bowles, Harry;Marriott, Heather;Jones, Ashley R.;Bouton, Clement R.;Dobson, Richard J. B.;Quinn, John P.;Al Khleifat, Ahmad;Swanson, Chad M.;Al-Chalabi, Ammar;Iacoangeli, Alfredo
Human endogenous retroviruses (HERVs) integrated into the human genome as a result of ancient exogenous infections and currently comprise ∼8% of our genome. The members of the most recently acquired HERV family, HERV-Ks, still retain the potential to produce viral molecules and have been linked to a wide range of diseases including cancer and neurodegeneration. Although a range of tools for HERV detection in NGS data exist, most of them lack wet lab validation and they do not cover all steps of the analysis. Here, we describe RetroSnake, an end-to-end, modular, computationally efficient, and customizable pipeline for the discovery of HERVs in short-read NGS data. RetroSnake is based on an extensively wet-lab validated protocol, it covers all steps of the analysis from raw data to the generation of annotated results presented as an interactive html file, and it is easy to use by life scientists without substantial computational training. Availability and implementation: The Pipeline and an extensive documentation are available on GitHub. RetroSnake is an end-to-end pipeline for detection of HERV-K insertions Modular and computationally efficient (∼4 h per genome) Easy setup and installation with Snakemake Can be installed and used by users with limited computational experience Bioinformatics; Biocomputational method; Sequence analysis
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DOI:
10.1093/bioinformatics/btq033
发表时间:
2010-03-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Quinlan AR;Hall IM
通讯作者:
Hall IM
影响因子:
14.9
作者:
Geoffroy V;Guignard T;Kress A;Gaillard JB;Solli-Nowlan T;Schalk A;Gatinois V;Dollfus H;Scheidecker S;Muller J
通讯作者:
Muller J
影响因子:
7
作者:
Gardner EJ;Lam VK;Harris DN;Chuang NT;Scott EC;Pittard WS;Mills RE;1000 Genomes Project Consortium;Devine SE
通讯作者:
Devine SE
影响因子:
4.8
作者:
Iacoangeli A;Fogh I;Selvackadunco S;Topp SD;Shatunov A;van Rheenen W;Al-Khleifat A;Opie-Martin S;Ratti A;Calvo A;UK Brain Expression Consortium;Van Damme P;Robberecht W;Chio A;Dobson RJ;Hardiman O;Shaw CE;van den Berg LH;Andersen PM;Smith BN;Silani V;Veldink JH;Breen G;Troakes C;Al-Chalabi A;Jones AR
通讯作者:
Jones AR
DOI:
10.1038/s41431-018-0177-4
发表时间:
2018-10
期刊:
European journal of human genetics : EJHG
影响因子:
--
作者:
Project MinE ALS Sequencing Consortium
通讯作者:
Project MinE ALS Sequencing Consortium