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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM1208977"><item key="SEX">male</item></item></item><item><item key="GSM1208977"><item key="SEX">male</item></item></item><item><item key="GSM1208977"><item key="SEX">male</item></item></item><item><item key="GSM1208974"><item key="SEX">female</item></item></item><item><item key="GSM1208974"><item key="SEX">female</item></item></item></item><item key="id">2016</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">The second trimester fetal transcriptome can be assessed based on cell-free RNA found within the amniotic fluid supernatant. The...</item><item key="geo_gse_id">E-GEOD-49891</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">5</item><item key="tags"><item>cell</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">rna-seq-and-expression-microarray-highlight-differ</item><item key="geo_id_plat">E-GEOD-49891_A-AFFY-44</item><item key="name">RNA-Seq and expression microarray highlight different aspects of the fetal amniotic fluid transcriptome [microarray]</item><item key="created">Jul.10, 2014</item><item key="summary">The second trimester fetal transcriptome can be assessed based on cell-free RNA found within the amniotic fluid supernatant. The objective of this study was to compare the suitability of two technologies for profiling the human fetal transcriptome: RNA-Seq and expression microarray. Comparisons were based on total numbers of gene detected, rank-order gene expression, and functional genomic analysis. Fewer gene transcripts were observed using RNA-Seq than microarray (4,158 vs 8,842). Correlation of total expression within each sample ranged from R=0.43 to R=0.57. On average, there was 59% concordance in gene identity among the top 10% of genes ranked by expression. The RNA-Seq data yielded more significant pathways enrichment within the ?Physiological Systems Development and Function? categories of IPA. Alternative splicing of many well-known genes, including those previously studied in fetal development, such as H19 and IGF2  is detected by RNA-Seq. Also included in this paper is discussion of the technical challenges inherent to working with cell-free fetal RNA and possible solutions. Cell-free fetal RNA from the amniotic fluid supernatant of five second trimester fetuses was divided and prepared in tandem for analysis using either the Illumina HiSeq 2000 or Affymetrix HG-U133 Plus 2.0 GeneChip microarray.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-49891</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-49891/samples/</item></data></biogps>
