<HashMap><database>EGA</database><scores/><additional><omics_type>Genomics</omics_type><dataset_type>Illumina HiSeq 2000;ILLUMINA</dataset_type><full_dataset_link>https://ega-archive.org/datasets/EGAD00001004034</full_dataset_link><sample_count>8</sample_count><description>EGA dataset EGAD00001004034</description><repository>EGA</repository><title>RNA-seq data from hypothalamic tissue from individuals with Prader-Willi syndrome and age-matched controls.</title><name_synonyms>Vasp, VASP, DmelCG15112, ENHANCER OF ATNSI ACTIVITY, Data Set, MENA, NDPP1, l(2)02029, Enb, enb, ENA, Ena, CG15112, 2018., ENA/VASP</name_synonyms><description_synonyms>Prader-Labhart-Willi, d230, BamF, bim, biml, Preoptico-Hypothalamic Area, short stature, BamC, bam, Prader Willi Syndrome, mental retardation, "Prader-Willi syndrome (disorder)" EXACT [SNOMEDCT_2005_07_31:89392001], dTAFII250, Lamina Terminalis, Labhart-Willi-Prader-Fanconi Syndrome, Prader-Labhart-Willi Syndrome, EfW1, prevention, fs(3)neo61, dmTAF[[II]]230, CG10422, Publication, dmTAF1, Taf230, PWS, Labhart Willi Prader Fanconi Syndrome, Whole Transcriptome Shotgun Sequencing, bim-beta7, DmelCG10422, prevention and control, intellectual disability, TAF250, Taf200, dTAF[[II]]250, reference sample, TFIID TAF250, "Prader-Willi syndrome" EXACT [ICD9CM_2006:759.81], HCAP, cel, bim-beta6, cell, Prader-Willi, Royer's, Taf1p, experimental design, CDLS3, BMH, Willi-Prader Syndrome, preventive measures, dTAF250, data processing, hypogonadotropic hypogonadism, Syndrome, Labhart Willi Syndrome, "Prader Willi syndrome" EXACT [CSP2005:1849-7731], Labhart-Willi, CSPG6, TAF, Controlled, Controlling, dTAF[[II]]230, TAF[[II]]250, preventive therapy, Prader-Willi syndrome chromosome region, RnBP, Preoptico-Hypothalamic Areas, TAF200, GlcNAc 2-epimerase, RNA-seq, l(3)84Ab, ham, BOD, BG:DS00004.13, TAFII-250, TAF250/230, Cell, obesity, Royers Syndrome, dTAF230, Royer's Syndrome, Royer Syndrome, N-acetyl-D-glucosamine 2-epimerase, TAFII250, p230, RENBP, Areas, TAF[[II]]250/230, Area, TFIID, muscular hypotonia, bod, bimel, Preoptico-Hypothalamic, and small hands and feet, Taf[[II]]250, TAF[[II]]230, prophylaxis, Preoptico Hypothalamic Area, Labhart-Willi-Prader-Fanconi, TAF[II]250, alpha, Prader Labhart Willi Syndrome, Willi-Prader, CG17603, TAF[[II]], Willi Prader Syndrome, Royer, AGE, "Prader - Willi syndrome" EXACT [SNOMEDCT_2005_07_31:205794007], data analysis, DmelCG17603, BIM, TAF1., Taf250, control, Bam-C, SR3-5, BAM, Bam, SMC3L1, Prader-Willi-like syndrome associated with chromosome 6, renin-binding protein, 2018, TAF230, hypothalamus, Labhart-Willi Syndrome</description_synonyms></additional><is_claimable>false</is_claimable><name>ena-DATASET-QMUL-Blizard-12-03-2018-09:10:11:257-296 - samples</name><description>RNA-seq data (bam files) from the hypothalamus of 4 individuals with Prader-Willi syndrome and 4 age-matched control individuals. Detailed information about the study design, case-control matching and RNA-seq data processing is provided in the accompanying publication [Bochukova et al (2018) Cell Reports].</description><dates><updated>2018-03-26 09:50:56</updated></dates><accession>EGAD00001004034</accession><cross_references><TAXONOMY>9606</TAXONOMY><EGA>EGAC00001000869</EGA><EGA>EGAS00001002901</EGA></cross_references></HashMap>