<HashMap><database>EVA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB27278/Craniosnyostotic_Rabbit_Colony_eva08062018.vcf.gz</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB27278/Craniosnyostotic_Rabbit_Colony_eva08062018.vcf.gz.tbi</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB27278/Craniosnyostotic_Rabbit_Colony_eva08062018.accessioned.vcf.gz</Vcf></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>0</viewCount><searchCount>0</searchCount></scores><additional><dataset_type>Genotyping By Array</dataset_type><omics_type>Genomics</omics_type><submitter>University of Pittsburgh/Children's Hospital of Pittsburgh of UPMC</submitter><instrument_platform>Illumina HiSeq 2000</instrument_platform><species>Oryctolagus Cuniculus</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJEB27278</full_dataset_link><repository>EVA</repository><name_synonyms>New, other disease, rabbits, European rabbit, Belgian Hare, NZW, Chinchilla Rabbits, Chinchilla, frequency, Zealand Rabbits, familial, disorders, Domestic Rabbits, medical condition, rabbit, Rabbits, NZW., diseases, Hare, Diseases, Belgian, New Zealand, disease or disorder, condition, diseases and disorders, Oryctolagus, Zealand Rabbit, outbreaks, Japanese white rabbit, NZW Rabbit, human disease, Rabbit, occurrence, New Zealand Rabbits, prevalence, New Zealand White Rabbits, Oryctolagus cuniculus, Age of onset, Domestic, Age symptoms begin, surveillance, New Zealand White Rabbit, NZW Rabbits, morbidity, endemics, Chinchilla Rabbit, genetic, non-neoplastic, domestic rabbit, disease, Domestic Rabbit, New Zealand Rabbit, cuniculus, disorder, Homo sapiens disease, epidemics, inherited genetic, Lepus cuniculus, constitutitional genetic, hereditary, incidence</name_synonyms><description_synonyms>symmetric dyschromatosis of the extremities, New, rabbits, European rabbit, CG42628, CG5692, Belgian Hare, NZW, Chinchilla Rabbits, Chinchilla, Zealand Rabbits, Domestic Rabbits, rapsyn, rad, rabbit, CG15720, DSH, Hospital, DmelCG5692, gDNA, Fs(3)Sz11, Rabbits, DmelCG42628, Hare, Belgian, New Zealand, University, Raps, DmF2, Oryctolagus, Zealand Rabbit, Fs(3)Hor, Pins, Japanese white rabbit, NZW Rabbit, lod, average, DmelCG2684, rsh, Rabbit, pins, ribosome-associated degradation, New Zealand Rabbits, New Zealand White Rabbits, familial reticulate acropigmentation of Dohi, Oryctolagus cuniculus, dyschromatosis symmetrica hereditaria 1, Dmel_CG15720, Age of onset, Domestic, Age symptoms begin, NTef2, Lds, New Zealand White Rabbit, NZW Rabbits, Children, PINS, early, Chinchilla Rabbit, domestic rabbit, Phenotypes, Domestic Rabbit, New Zealand Rabbit, Horka, cuniculus, CG2684, CG4346, Fs(3)Horka, REM3., RAD, Rad, Lepus cuniculus, RAD1, Dmel_CG4346</description_synonyms><citation_count>0</citation_count></additional><is_claimable>false</is_claimable><name>Genetic Basis for Disease Occurrence and Onset in the Craniosynostotic Rabbit</name><description>Genomic DNA was isolated from rabbits with normal, delayed-onset synostotic, and early-onset synostotic phenotypes maintained in a colony at the University of Pittsburgh/Children's Hospital of Pittsburgh. Samples were submitted to Floragenex (Portland, OR) for RAD-sequencing and variant calling.</description><dates><publication>2018-06-13</publication></dates><accession>PRJEB27278</accession><cross_references><TAXONOMY>9986</TAXONOMY></cross_references></HashMap>