The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

Detalhes bibliográficos
Autor(a) principal: Buxbaum, J.D.
Data de Publicação: 2014
Outros Autores: Bolshakova, N., Brownfeld, J.M., Anney, R.J., Bender, P., Bernier, R., Cook, E.H., Coon, H., Cuccaro, M., Freitag, C.M., Hallmayer, J., Geschwind, D, Klauck, S.M., Nurnberger, J.I., Oliveira, G., Pinto, D., Poustka, F., Scherer, W.S., Shih, A., Sutcliffe, J.S., Szatmari, P., Vicente, A.M., Vieland, V., Gallagher, L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.18/2465
Resumo: BACKGROUND: There is an urgent need for expanding and enhancing autism spectrum disorder (ASD) samples, in order to better understand causes of ASD. METHODS: In a unique public-private partnership, 13 sites with extensive experience in both the assessment and diagnosis of ASD embarked on an ambitious, 2-year program to collect samples for genetic and phenotypic research and begin analyses on these samples. The program was called The Autism Simplex Collection (TASC). TASC sample collection began in 2008 and was completed in 2010, and included nine sites from North America and four sites from Western Europe, as well as a centralized Data Coordinating Center. RESULTS: Over 1,700 trios are part of this collection, with DNA from transformed cells now available through the National Institute of Mental Health (NIMH). Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedule-Generic (ADOS-G) measures are available for all probands, as are standardized IQ measures, Vineland Adaptive Behavioral Scales (VABS), the Social Responsiveness Scale (SRS), Peabody Picture Vocabulary Test (PPVT), and physical measures (height, weight, and head circumference). At almost every site, additional phenotypic measures were collected, including the Broad Autism Phenotype Questionnaire (BAPQ) and Repetitive Behavior Scale-Revised (RBS-R), as well as the non-word repetition scale, Communication Checklist (Children's or Adult), and Aberrant Behavior Checklist (ABC). Moreover, for nearly 1,000 trios, the Autism Genome Project Consortium (AGP) has carried out Illumina 1 M SNP genotyping and called copy number variation (CNV) in the samples, with data being made available through the National Institutes of Health (NIH). Whole exome sequencing (WES) has been carried out in over 500 probands, together with ancestry matched controls, and this data is also available through the NIH. Additional WES is being carried out by the Autism Sequencing Consortium (ASC), where the focus is on sequencing complete trios. ASC sequencing for the first 1,000 samples (all from whole-blood DNA) is complete and data will be released in 2014. Data is being made available through NIH databases (database of Genotypes and Phenotypes (dbGaP) and National Database for Autism Research (NDAR)) with DNA released in Dist 11.0. Primary funding for the collection, genotyping, sequencing and distribution of TASC samples was provided by Autism Speaks and the NIH, including the National Institute of Mental Health (NIMH) and the National Human Genetics Research Institute (NHGRI). CONCLUSIONS: TASC represents an important sample set that leverages expert sites. Similar approaches, leveraging expert sites and ongoing studies, represent an important path towards further enhancing available ASD samples.
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spelling The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analysesPerturbações do Desenvolvimento Infantil e Saúde MentalAutismSaúde PúblicaPortugalBACKGROUND: There is an urgent need for expanding and enhancing autism spectrum disorder (ASD) samples, in order to better understand causes of ASD. METHODS: In a unique public-private partnership, 13 sites with extensive experience in both the assessment and diagnosis of ASD embarked on an ambitious, 2-year program to collect samples for genetic and phenotypic research and begin analyses on these samples. The program was called The Autism Simplex Collection (TASC). TASC sample collection began in 2008 and was completed in 2010, and included nine sites from North America and four sites from Western Europe, as well as a centralized Data Coordinating Center. RESULTS: Over 1,700 trios are part of this collection, with DNA from transformed cells now available through the National Institute of Mental Health (NIMH). Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedule-Generic (ADOS-G) measures are available for all probands, as are standardized IQ measures, Vineland Adaptive Behavioral Scales (VABS), the Social Responsiveness Scale (SRS), Peabody Picture Vocabulary Test (PPVT), and physical measures (height, weight, and head circumference). At almost every site, additional phenotypic measures were collected, including the Broad Autism Phenotype Questionnaire (BAPQ) and Repetitive Behavior Scale-Revised (RBS-R), as well as the non-word repetition scale, Communication Checklist (Children's or Adult), and Aberrant Behavior Checklist (ABC). Moreover, for nearly 1,000 trios, the Autism Genome Project Consortium (AGP) has carried out Illumina 1 M SNP genotyping and called copy number variation (CNV) in the samples, with data being made available through the National Institutes of Health (NIH). Whole exome sequencing (WES) has been carried out in over 500 probands, together with ancestry matched controls, and this data is also available through the NIH. Additional WES is being carried out by the Autism Sequencing Consortium (ASC), where the focus is on sequencing complete trios. ASC sequencing for the first 1,000 samples (all from whole-blood DNA) is complete and data will be released in 2014. Data is being made available through NIH databases (database of Genotypes and Phenotypes (dbGaP) and National Database for Autism Research (NDAR)) with DNA released in Dist 11.0. Primary funding for the collection, genotyping, sequencing and distribution of TASC samples was provided by Autism Speaks and the NIH, including the National Institute of Mental Health (NIMH) and the National Human Genetics Research Institute (NHGRI). CONCLUSIONS: TASC represents an important sample set that leverages expert sites. Similar approaches, leveraging expert sites and ongoing studies, represent an important path towards further enhancing available ASD samples.BioMed CentralRepositório Científico do Instituto Nacional de SaúdeBuxbaum, J.D.Bolshakova, N.Brownfeld, J.M.Anney, R.J.Bender, P.Bernier, R.Cook, E.H.Coon, H.Cuccaro, M.Freitag, C.M.Hallmayer, J.Geschwind, DKlauck, S.M.Nurnberger, J.I.Oliveira, G.Pinto, D.Poustka, F.Scherer, W.S.Shih, A.Sutcliffe, J.S.Szatmari, P.Vicente, A.M.Vieland, V.Gallagher, L.2014-11-26T17:07:39Z2014-05-202014-05-20T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/2465engMol Autism. 2014 May 20;5:34. doi: 10.1186/2040-2392-5-34. eCollection 2014.2040-239210.1186/2040-2392-5-34info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:39:18Zoai:repositorio.insa.pt:10400.18/2465Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:37:29.308625Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
title The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
spellingShingle The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
Buxbaum, J.D.
Perturbações do Desenvolvimento Infantil e Saúde Mental
Autism
Saúde Pública
Portugal
title_short The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
title_full The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
title_fullStr The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
title_full_unstemmed The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
title_sort The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
author Buxbaum, J.D.
author_facet Buxbaum, J.D.
Bolshakova, N.
Brownfeld, J.M.
Anney, R.J.
Bender, P.
Bernier, R.
Cook, E.H.
Coon, H.
Cuccaro, M.
Freitag, C.M.
Hallmayer, J.
Geschwind, D
Klauck, S.M.
Nurnberger, J.I.
Oliveira, G.
Pinto, D.
Poustka, F.
Scherer, W.S.
Shih, A.
Sutcliffe, J.S.
Szatmari, P.
Vicente, A.M.
Vieland, V.
Gallagher, L.
author_role author
author2 Bolshakova, N.
Brownfeld, J.M.
Anney, R.J.
Bender, P.
Bernier, R.
Cook, E.H.
Coon, H.
Cuccaro, M.
Freitag, C.M.
Hallmayer, J.
Geschwind, D
Klauck, S.M.
Nurnberger, J.I.
Oliveira, G.
Pinto, D.
Poustka, F.
Scherer, W.S.
Shih, A.
Sutcliffe, J.S.
Szatmari, P.
Vicente, A.M.
Vieland, V.
Gallagher, L.
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.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Buxbaum, J.D.
Bolshakova, N.
Brownfeld, J.M.
Anney, R.J.
Bender, P.
Bernier, R.
Cook, E.H.
Coon, H.
Cuccaro, M.
Freitag, C.M.
Hallmayer, J.
Geschwind, D
Klauck, S.M.
Nurnberger, J.I.
Oliveira, G.
Pinto, D.
Poustka, F.
Scherer, W.S.
Shih, A.
Sutcliffe, J.S.
Szatmari, P.
Vicente, A.M.
Vieland, V.
Gallagher, L.
dc.subject.por.fl_str_mv Perturbações do Desenvolvimento Infantil e Saúde Mental
Autism
Saúde Pública
Portugal
topic Perturbações do Desenvolvimento Infantil e Saúde Mental
Autism
Saúde Pública
Portugal
description BACKGROUND: There is an urgent need for expanding and enhancing autism spectrum disorder (ASD) samples, in order to better understand causes of ASD. METHODS: In a unique public-private partnership, 13 sites with extensive experience in both the assessment and diagnosis of ASD embarked on an ambitious, 2-year program to collect samples for genetic and phenotypic research and begin analyses on these samples. The program was called The Autism Simplex Collection (TASC). TASC sample collection began in 2008 and was completed in 2010, and included nine sites from North America and four sites from Western Europe, as well as a centralized Data Coordinating Center. RESULTS: Over 1,700 trios are part of this collection, with DNA from transformed cells now available through the National Institute of Mental Health (NIMH). Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedule-Generic (ADOS-G) measures are available for all probands, as are standardized IQ measures, Vineland Adaptive Behavioral Scales (VABS), the Social Responsiveness Scale (SRS), Peabody Picture Vocabulary Test (PPVT), and physical measures (height, weight, and head circumference). At almost every site, additional phenotypic measures were collected, including the Broad Autism Phenotype Questionnaire (BAPQ) and Repetitive Behavior Scale-Revised (RBS-R), as well as the non-word repetition scale, Communication Checklist (Children's or Adult), and Aberrant Behavior Checklist (ABC). Moreover, for nearly 1,000 trios, the Autism Genome Project Consortium (AGP) has carried out Illumina 1 M SNP genotyping and called copy number variation (CNV) in the samples, with data being made available through the National Institutes of Health (NIH). Whole exome sequencing (WES) has been carried out in over 500 probands, together with ancestry matched controls, and this data is also available through the NIH. Additional WES is being carried out by the Autism Sequencing Consortium (ASC), where the focus is on sequencing complete trios. ASC sequencing for the first 1,000 samples (all from whole-blood DNA) is complete and data will be released in 2014. Data is being made available through NIH databases (database of Genotypes and Phenotypes (dbGaP) and National Database for Autism Research (NDAR)) with DNA released in Dist 11.0. Primary funding for the collection, genotyping, sequencing and distribution of TASC samples was provided by Autism Speaks and the NIH, including the National Institute of Mental Health (NIMH) and the National Human Genetics Research Institute (NHGRI). CONCLUSIONS: TASC represents an important sample set that leverages expert sites. Similar approaches, leveraging expert sites and ongoing studies, represent an important path towards further enhancing available ASD samples.
publishDate 2014
dc.date.none.fl_str_mv 2014-11-26T17:07:39Z
2014-05-20
2014-05-20T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.18/2465
url http://hdl.handle.net/10400.18/2465
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Mol Autism. 2014 May 20;5:34. doi: 10.1186/2040-2392-5-34. eCollection 2014.
2040-2392
10.1186/2040-2392-5-34
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv BioMed Central
publisher.none.fl_str_mv BioMed Central
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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