[{"name": "A Whole Genome Approach to Characterising a Novel Immunodeficiency Disorder", "sample_count": 2, "tags": ["genome", "nucleotide", "peripheral", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-14845", "id": 3171, "slug": "a-whole-genome-approach-to-characterising-a-novel", "factor_count": 1}, {"name": "BCOR-regulated genes in human oculo-facio-cardio-dental syndrome", "sample_count": 2, "tags": ["apical", "eye", "genetic disorder", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-15214", "id": 3211, "slug": "bcor-regulated-genes-in-human-oculo-facio-cardio-d", "factor_count": 0}, {"name": "Common gene expression profile in the mitochondrial syndrome of coenzyme Q deficiency", "sample_count": 15, "tags": ["disease", "fibroblast", "lipid", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-33769", "id": 2475, "slug": "common-gene-expression-profile-in-the-mitochondria", "factor_count": 5}, {"name": "Common Gene Transcriptional Patterns Following Immobilization, Spinal Cord Injury, and Unloading in Human Skeletal Muscle", "sample_count": 20, "tags": ["autoimmune disease", "brain", "compartment", "compartment syndrome", "disease", "liquid", "muscle", "protein", "spinal cord", "syndrome", "vastus lateralis"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-21497", "id": 3642, "slug": "common-gene-transcriptional-patterns-following-imm", "factor_count": 1}, {"name": "Correlated alterations in genome organization, histone methylation, and DNA-lamina interactions in Hutchinson-Gilford progeria syndrome (expression)", "sample_count": 6, "tags": ["chromatin", "chromosome", "disease", "exon", "genome", "heterochromatin", "hutchinson-gilford progeria syndrome", "lamin a", "nuclear lamin", "nuclear lamina", "point", "protein", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-41751", "id": 4601, "slug": "correlated-alterations-in-genome-organization-hist", "factor_count": 4}, {"name": "Differential Gene Expression in Granulosa Cells from Polycystic Ovary Syndrome Patients with and without Insulin Resistance:  Identification of Susceptibility Gene Sets through Network Analysis", "sample_count": 10, "tags": ["ovary", "polycystic ovary syndrome", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-34526", "id": 2699, "slug": "differential-gene-expression-in-granulosa-cells-fr", "factor_count": 1}, {"name": "Expression data of ribosomal proteins from sorted hematopoietic stems cells from patients with low risk MDS.", "sample_count": 19, "tags": ["myelodysplastic syndrome", "protein", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-30201", "id": 4144, "slug": "expression-data-of-ribosomal-proteins-from-sorted", "factor_count": 2}, {"name": "Expression data of the iPSCs derived from foreskin fibroblast cells of normal person and KS patient", "sample_count": 18, "tags": ["chromosome", "disease", "fibroblast", "line", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-37258", "id": 4465, "slug": "expression-data-of-the-ipscs-derived-from-foreskin", "factor_count": 3}, {"name": "Expression profiles of amniotic fluid from human fetuses with Down syndrome and euploid controls", "sample_count": 14, "tags": ["chromosome", "down syndrome", "protein", "syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-16176", "id": 3286, "slug": "expression-profiles-of-amniotic-fluid-from-human-f", "factor_count": 3}, {"name": "Expression profiling in Williams-Beuren Syndrome patient fibroblast cell lines", "sample_count": 17, "tags": ["cell", "chromosome", "disease", "fibroblast", "serum", "skin", "syndrome", "williams-beuren syndrome"], "species": "human", "is_default": false, "geo_gse_id": "E-GEOD-16715", "id": 3327, "slug": "expression-profiling-in-williams-beuren-syndrome-p", "factor_count": 2}]