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Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: A virtual appliance approach for instant deployment

Title: Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: A virtual appliance approach for instant deployment
Authors: Li, Jason; Doyle, Maria A; Saeed, Isaam; Wong, Stephen Q; Mar, Victoria; Goode, David; Caramia, Franco; Doig, Kenneth D; Ryland, Georgina L; Thompson, Ella R; Hunter, Sally M; Halgamuge, Saman Kumara; Ellul, Jason; Dobrovic, Alexander; Campbell, Ian G; Papenfuss, Anthony Troy; McArthur, Grant A; Tothill, Richard
Source: Li, J, Doyle, M A, Saeed, I, Wong, S Q, Mar, V, Goode, D, Caramia, F, Doig, K D, Ryland, G L, Thompson, E R, Hunter, S M, Halgamuge, S K, Ellul, J, Dobrovic, A, Campbell, I G, Papenfuss, A T, McArthur, G A & Tothill, R 2014, 'Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: A virtual appliance approach for instant deployment', PLoS ONE, vol. 9, no. 4, e95217. https://doi.org/10.1371/journal.pone.0095217
Publication Year: 2014
Description: Targeted resequencing by massively parallel sequencing has become an effective and affordable way to survey small to large portions of the genome for genetic variation. Despite the rapid development in open source software for analysis of such data, the practical implementation of these tools through construction of sequencing analysis pipelines still remains a challenging and laborious activity, and a major hurdle for many small research and clinical laboratories. We developed TREVA (Targeted REsequencing Virtual Appliance), making pre-built pipelines immediately available as a virtual appliance. Based on virtual machine technologies, TREVA is a solution for rapid and efficient deployment of complex bioinformatics pipelines to laboratories of all sizes, enabling reproducible results. The analyses that are supported in TREVA include: somatic and germline single-nucleotide and insertion/deletion variant calling, copy number analysis, and cohort-based analyses such as pathway and significantly mutated genes analyses. TREVA is flexible and easy to use, and can be customised by Linux-based extensions if required. TREVA can also be deployed on the cloud (cloud computing), enabling instant access without investment overheads for additional hardware. TREVA is available at http://bioinformatics. petermac.org/treva/.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
ISSN: 1932-6203
Relation: info:eu-repo/semantics/altIdentifier/wos/000335227400041; info:eu-repo/semantics/altIdentifier/pissn/1932-6203; info:eu-repo/semantics/altIdentifier/eissn/1932-6203
DOI: 10.1371/journal.pone.0095217
Availability: https://research.monash.edu/en/publications/72d33c03-79f7-490e-ada5-34af5f5fbb0b; https://doi.org/10.1371/journal.pone.0095217; https://researchmgt.monash.edu/ws/files/232927315/2458765_oa.pdf; http://www.plosone.org/article/fetchObject.action?uri=info%3Adoi%2F10.1371%2Fjournal.pone.0095217&representation=PDF; https://www.scopus.com/pages/publications/84899697726
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.30A15109
Database: BASE