{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,20]],"date-time":"2026-07-20T19:29:42Z","timestamp":1784575782516,"version":"3.55.0"},"reference-count":6,"publisher":"Oxford University Press (OUP)","issue":"4","license":[{"start":{"date-parts":[[2018,8,8]],"date-time":"2018-08-08T00:00:00Z","timestamp":1533686400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"BBSRC LiDO PHD studentship"},{"name":"Bloomsbury Research Fund PhD studentship"},{"DOI":"10.13039\/501100000265","name":"MRC","doi-asserted-by":"publisher","award":["MR\/K000551\/1"],"award-info":[{"award-number":["MR\/K000551\/1"]}],"id":[{"id":"10.13039\/501100000265","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100000265","name":"MRC","doi-asserted-by":"publisher","award":["MR\/M01360X\/1"],"award-info":[{"award-number":["MR\/M01360X\/1"]}],"id":[{"id":"10.13039\/501100000265","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100000265","name":"MRC","doi-asserted-by":"publisher","award":["MR\/N010469\/1"],"award-info":[{"award-number":["MR\/N010469\/1"]}],"id":[{"id":"10.13039\/501100000265","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,2,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Summary<\/jats:title>\n                  <jats:p>Recombinase polymerase amplification (RPA), an isothermal nucleic acid amplification method, is enhancing our ability to detect a diverse array of pathogens, thereby assisting the diagnosis of infectious diseases and the detection of microorganisms in food and water. However, new bioinformatics tools are needed to automate and improve the design of the primers and probes sets to be used in RPA, particularly to account for the high genetic diversity of circulating pathogens and cross detection of genetically similar organisms. PrimedRPA is a python-based package that automates the creation and filtering of RPA primers and probe sets. It aligns several sequences to identify conserved targets, and filters regions that cross react with possible background organisms.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Availability and implementation<\/jats:title>\n                  <jats:p>PrimedRPA was implemented in Python 3 and supported on Linux and MacOS and is freely available from http:\/\/pathogenseq.lshtm.ac.uk\/PrimedRPA.html.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Supplementary information<\/jats:title>\n                  <jats:p>Supplementary data are available at Bioinformatics online.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/bioinformatics\/bty701","type":"journal-article","created":{"date-parts":[[2018,8,7]],"date-time":"2018-08-07T19:12:59Z","timestamp":1533669179000},"page":"682-684","source":"Crossref","is-referenced-by-count":84,"title":["PrimedRPA: primer design for recombinase polymerase amplification assays"],"prefix":"10.1093","volume":"35","author":[{"given":"Matthew","family":"Higgins","sequence":"first","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7818-2348","authenticated-orcid":false,"given":"Matt","family":"Ravenhall","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel","family":"Ward","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8323-7019","authenticated-orcid":false,"given":"Jody","family":"Phelan","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amy","family":"Ibrahim","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthew S","family":"Forrest","sequence":"additional","affiliation":[{"name":"TwistDx, Coldhams Business Park, Cambridge, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Taane G","family":"Clark","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"},{"name":"Department of Infectious Disease Epidemiology, LSHTM, London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1403-6138","authenticated-orcid":false,"given":"Susana","family":"Campino","sequence":"additional","affiliation":[{"name":"Pathogen Molecular Biology Department, London School of Hygiene and Tropical Medicine (LSHTM), London, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2018,8,8]]},"reference":[{"key":"2023051511005773100_bty701-B1","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1186\/s12879-015-1212-5","article-title":"Development of a rapid recombinase polymerase amplification assay for the detection of Streptococcus pneumoniae in whole blood","volume":"15","author":"Clancy","year":"2015","journal-title":"BMC Infect. 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