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URL: https://sfari.org/resources/simons-simplex-collection
Proper Citation: Simons Simplex Collection (RRID:SCR_004644)
Description: Repository of genetic samples from approximately 3,000 families, each of which has one child affected with an Autism Spectrum Disorder (ASD) and parents unaffected with ASD. A central database characterizing all of the study subjects is available to any qualified researcher and biospecimens are freely available to SFARI grant holders, and to other researchers on a modest fee-for-use basis. Each genetic sample will have an associated collection of data that provides a precise characterization of the individual (phenotype). Rigorous phenotyping will maximize the value of the resource for a wide variety of future research projects into the causes and mechanisms of autism. The Simons Simplex Collection is operated by SFARI in collaboration with twelve university-affiliated research clinics.
Abbreviations: SSC
Resource Type: biomaterial supply resource, cell repository, material resource
Keywords: phenotype, genetic, cell line, fibroblast, dna, plasma
Related Condition: Autism, Autism Spectrum Disorder, Unaffected parent
Availability: Public: Central database is available to any qualified researcher and biospecimens are freely available to SFARI grant holders, And to other researchers on a modest fee-for-use basis.
Resource Name: Simons Simplex Collection
Resource ID: SCR_004644
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400