Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples

Autores
Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; Valas, Stephen; Brnić, Dragan; Jungić, Andreja; Ruano, María José; Sánchez, Azucena; Murakami, Kenji; Nakamura, Kurumi; Puentes, Rodrigo; De Brun, MLaureana; Ruiz, Vanesa; Ladera Gomez, Marla Eliana; Lendez, Pamela Anahí; Dolcini, Guillermina Laura; Camargos, Marcelo Fernandes; Fonseca, Antônio; Barua, Subarna; Wang, Chengming; Giza, Aleksandra; Kuźmak, Jacek
Año de publicación
2024
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.
Fil: Pluta, Aneta. National Veterinary Research Institute; Polonia
Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Droscha, Casey. CentralStar Cooperative; Estados Unidos
Fil: VanderWeele, Sophie. CentralStar Cooperative; Estados Unidos
Fil: Taxis, Tasia M.. Michigan State University; Estados Unidos
Fil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; Francia
Fil: Brnić, Dragan. Croatian Veterinary Institute; Croacia
Fil: Jungić, Andreja. Croatian Veterinary Institute; Croacia
Fil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; España
Fil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; España
Fil: Murakami, Kenji. Iwate University; Japón
Fil: Nakamura, Kurumi. Iwate University; Japón
Fil: Puentes, Rodrigo. Universidad de la República; Uruguay
Fil: De Brun, MLaureana. Universidad de la República; Uruguay
Fil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Barua, Subarna. Auburn University.; Estados Unidos
Fil: Wang, Chengming. Auburn University.; Estados Unidos
Fil: Giza, Aleksandra. National Veterinary Research Institute; Polonia
Fil: Kuźmak, Jacek. National Veterinary Research Institute; Polonia
Materia
LEUCEMIA BOVINA
BLV
qPCR
DIAGNOSTICO
VALIDACION
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/266801

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network_name_str CONICET Digital (CONICET)
spelling Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samplesPluta, AnetaJaworski, Juan PabloDroscha, CaseyVanderWeele, SophieTaxis, Tasia M.Valas, StephenBrnić, DraganJungić, AndrejaRuano, María JoséSánchez, AzucenaMurakami, KenjiNakamura, KurumiPuentes, RodrigoDe Brun, MLaureanaRuiz, VanesaLadera Gomez, Marla ElianaLendez, Pamela AnahíDolcini, Guillermina LauraCamargos, Marcelo FernandesFonseca, AntônioBarua, SubarnaWang, ChengmingGiza, AleksandraKuźmak, JacekLEUCEMIA BOVINABLVqPCRDIAGNOSTICOVALIDACIONhttps://purl.org/becyt/ford/4.3https://purl.org/becyt/ford/4Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.Fil: Pluta, Aneta. National Veterinary Research Institute; PoloniaFil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; ArgentinaFil: Droscha, Casey. CentralStar Cooperative; Estados UnidosFil: VanderWeele, Sophie. CentralStar Cooperative; Estados UnidosFil: Taxis, Tasia M.. Michigan State University; Estados UnidosFil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; FranciaFil: Brnić, Dragan. Croatian Veterinary Institute; CroaciaFil: Jungić, Andreja. Croatian Veterinary Institute; CroaciaFil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; EspañaFil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; EspañaFil: Murakami, Kenji. Iwate University; JapónFil: Nakamura, Kurumi. Iwate University; JapónFil: Puentes, Rodrigo. Universidad de la República; UruguayFil: De Brun, MLaureana. Universidad de la República; UruguayFil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; ArgentinaFil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; ArgentinaFil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; BrasilFil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; BrasilFil: Barua, Subarna. Auburn University.; Estados UnidosFil: Wang, Chengming. Auburn University.; Estados UnidosFil: Giza, Aleksandra. National Veterinary Research Institute; PoloniaFil: Kuźmak, Jacek. National Veterinary Research Institute; PoloniaBioMed Central2024-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/266801Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-191746-6148CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://bmcvetres.biomedcentral.com/articles/10.1186/s12917-024-04228-zinfo:eu-repo/semantics/altIdentifier/doi/10.1186/s12917-024-04228-zinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:57:50Zoai:ri.conicet.gov.ar:11336/266801instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:57:50.844CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
title Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
spellingShingle Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
Pluta, Aneta
LEUCEMIA BOVINA
BLV
qPCR
DIAGNOSTICO
VALIDACION
title_short Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
title_full Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
title_fullStr Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
title_full_unstemmed Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
title_sort Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples
dc.creator.none.fl_str_mv Pluta, Aneta
Jaworski, Juan Pablo
Droscha, Casey
VanderWeele, Sophie
Taxis, Tasia M.
Valas, Stephen
Brnić, Dragan
Jungić, Andreja
Ruano, María José
Sánchez, Azucena
Murakami, Kenji
Nakamura, Kurumi
Puentes, Rodrigo
De Brun, MLaureana
Ruiz, Vanesa
Ladera Gomez, Marla Eliana
Lendez, Pamela Anahí
Dolcini, Guillermina Laura
Camargos, Marcelo Fernandes
Fonseca, Antônio
Barua, Subarna
Wang, Chengming
Giza, Aleksandra
Kuźmak, Jacek
author Pluta, Aneta
author_facet Pluta, Aneta
Jaworski, Juan Pablo
Droscha, Casey
VanderWeele, Sophie
Taxis, Tasia M.
Valas, Stephen
Brnić, Dragan
Jungić, Andreja
Ruano, María José
Sánchez, Azucena
Murakami, Kenji
Nakamura, Kurumi
Puentes, Rodrigo
De Brun, MLaureana
Ruiz, Vanesa
Ladera Gomez, Marla Eliana
Lendez, Pamela Anahí
Dolcini, Guillermina Laura
Camargos, Marcelo Fernandes
Fonseca, Antônio
Barua, Subarna
Wang, Chengming
Giza, Aleksandra
Kuźmak, Jacek
author_role author
author2 Jaworski, Juan Pablo
Droscha, Casey
VanderWeele, Sophie
Taxis, Tasia M.
Valas, Stephen
Brnić, Dragan
Jungić, Andreja
Ruano, María José
Sánchez, Azucena
Murakami, Kenji
Nakamura, Kurumi
Puentes, Rodrigo
De Brun, MLaureana
Ruiz, Vanesa
Ladera Gomez, Marla Eliana
Lendez, Pamela Anahí
Dolcini, Guillermina Laura
Camargos, Marcelo Fernandes
Fonseca, Antônio
Barua, Subarna
Wang, Chengming
Giza, Aleksandra
Kuźmak, Jacek
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv LEUCEMIA BOVINA
BLV
qPCR
DIAGNOSTICO
VALIDACION
topic LEUCEMIA BOVINA
BLV
qPCR
DIAGNOSTICO
VALIDACION
purl_subject.fl_str_mv https://purl.org/becyt/ford/4.3
https://purl.org/becyt/ford/4
dc.description.none.fl_txt_mv Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.
Fil: Pluta, Aneta. National Veterinary Research Institute; Polonia
Fil: Jaworski, Juan Pablo. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Droscha, Casey. CentralStar Cooperative; Estados Unidos
Fil: VanderWeele, Sophie. CentralStar Cooperative; Estados Unidos
Fil: Taxis, Tasia M.. Michigan State University; Estados Unidos
Fil: Valas, Stephen. French Agency for Food, Environmental and Occupational Health and Safety; Francia
Fil: Brnić, Dragan. Croatian Veterinary Institute; Croacia
Fil: Jungić, Andreja. Croatian Veterinary Institute; Croacia
Fil: Ruano, María José. Ministry of Agriculture, Fisheries and Food; España
Fil: Sánchez, Azucena. Ministry of Agriculture, Fisheries and Food; España
Fil: Murakami, Kenji. Iwate University; Japón
Fil: Nakamura, Kurumi. Iwate University; Japón
Fil: Puentes, Rodrigo. Universidad de la República; Uruguay
Fil: De Brun, MLaureana. Universidad de la República; Uruguay
Fil: Ruiz, Vanesa. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina
Fil: Ladera Gomez, Marla Eliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Lendez, Pamela Anahí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Dolcini, Guillermina Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigación Veterinaria de Tandil. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigación Veterinaria de Tandil. Provincia de Buenos Aires. Gobernación. Comision de Investigaciones Científicas. Centro de Investigación Veterinaria de Tandil; Argentina
Fil: Camargos, Marcelo Fernandes. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Fonseca, Antônio. Laboratório Federal de Defesa Agropecuária de Minas Gerais; Brasil
Fil: Barua, Subarna. Auburn University.; Estados Unidos
Fil: Wang, Chengming. Auburn University.; Estados Unidos
Fil: Giza, Aleksandra. National Veterinary Research Institute; Polonia
Fil: Kuźmak, Jacek. National Veterinary Research Institute; Polonia
description Bovine leukemia virus (BLV) is the etiological agent of enzootic bovine leukosis and causes a persistent infection that can leave cattle with no symptoms. Many countries have been able to successfully eradicate BLV through improved detection and management methods. However, with the increasing novel molecular detection methods there have been few eforts to standardize these results at global scale. This study aimed to determine the interlaboratory accuracy and agreement of 11 molecular tests in detecting BLV. Each qPCR/ddPCR method varied by target gene, primer design, DNA input and chemistries. DNA samples were extracted from blood of BLV-seropositive cattle and lyophilized to grant a better preservation during shipping to all participants around the globe. Twenty nine out of 44 samples were correctly identifed by the 11 labs and all methods exhibited a diagnostic sensitivity between 74 and 100%. Agreement amongst diferent assays was linked to BLV copy numbers present in samples and the characteristics of each assay (i.e., BLV target sequence). Finally, the mean correlation value for all assays was within the range of strong correlation. This study highlights the importance of continuous need for standardization and harmonization amongst assays and the diferent participants. The results underscore the need of an international calibrator to estimate the efciency (standard curve) of the diferent assays and improve quantitation accuracy. Additionally, this will inform future participants about the variability associated with emerging chemistries, methods, and technologies used to study BLV. Altogether, by improving tests performance worldwide it will positively aid in the eradication eforts.
publishDate 2024
dc.date.none.fl_str_mv 2024-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/266801
Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-19
1746-6148
CONICET Digital
CONICET
url http://hdl.handle.net/11336/266801
identifier_str_mv Pluta, Aneta; Jaworski, Juan Pablo; Droscha, Casey; VanderWeele, Sophie; Taxis, Tasia M.; et al.; Inter-laboratory comparison of eleven quantitative or digital PCR assays for detection of proviral bovine leukemia virus in blood samples; BioMed Central; BMC Veterinary Research; 20; 1; 8-2024; 1-19
1746-6148
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
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publisher.none.fl_str_mv BioMed Central
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