{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR988/004/ERR9888084/ERR9888084_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/001/ERR9896531/ERR9896531.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/002/ERR9896532/ERR9896532.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/005/ERR9890755/ERR9890755_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR988/004/ERR9888084/ERR9888084_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/003/ERR9896533/ERR9896533.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR989/005/ERR9890755/ERR9890755_2.fastq.gz"]},"type":"primary"},"statusCodeValue":200,"statusCode":"OK"}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Max Planck Institute for Evolutionary Anthropology"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJEB53912"],"long_description":["The Greek colony of Himera lasted from 648 BCE until its destruction by Carthage in 409 BCE and is one of the most extensively excavated cities from the Greek archaic / classical world. The skeletal remains belonging to a single male individual showing morphological indications of dwarfism were found in 2009 in the Western Necropolis of Himera in Sicily. Genetic analysis of genome-wide data generated for this individual confirmed the diagnosis of achondroplasia. This individual had entirely Anatolian ancestry."],"repository":["ENA"],"name_synonyms":["\"Chondrodystrophia\" EXACT [MTHICD9_2006:756.4], \"Achondroplasia (disorder)\" EXACT [SNOMEDCT_2005_07_31:86268005], Skeleton Skin Brain Syndrome, Skeleton-Skin-Brain Syndromes, set of bones of body, Skeleton-Skin-Brain, \"Achondroplastic physique\" EXACT [SNOMEDCT_2005_07_31:190584003], SADDAN Dysplasia, SADDAN Dysplasias, determination, Skeleton-Skin-Brain Syndrome, skeleton, Skeletons, Set of all bones, \"Achondroplastic dwarf\" EXACT [SNOMEDCT_2005_07_31:205467007], Dysplasias, Dysplasia, Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans, ACH, skeleton component, Syndromes, set of all bones, \"osteosclerosis congenita\" EXACT [CSP2005:2715-2940], SADDAN, \"achondroplasia\" EXACT [CSP2005:1849-0171]., chemical analysis, Syndrome, \"Achondroplastic dwarf\" EXACT [SNOMEDCT_2005_07_31:268273004], Achondroplasias, Achondroplasia, Achondroplastic dwarfism, With Developmental Delay And Acanthosis Nigricans, assay, \"Achondroplastic physique (finding)\" EXACT [SNOMEDCT_2005_07_31:248299001], SADDANs, Severe, Skelettsystem, Skeleton (in vivo), Set of bones of body"],"additional_accession":[]},"is_claimable":false,"name":"Genomic analysis of 5th century BCE skeleton from Himera, Sicily, reveals confirmed case of achondroplasia","description":"An achondroplastic individual from 5 th century BCE Himera, Sicily","dates":{"last_updated":"2024-06-04","first_public":"2024-06-04"},"accession":"PRJEB53912","cross_references":{}}