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authorBonface2024-02-09 09:41:28 -0600
committerMunyoki Kilyungi2024-08-09 13:30:43 +0300
commitd029d5d7f8ead1f1de8d318045004a4a6f68f5fb (patch)
tree33c7ff40e3f953d030ed08f468f7afb1dfcba9e6 /general/datasets/UTHSC_BXD_Hip_PostD7EtohBS_1121/summary.rtf
parent769ff7825f5d8d36d541e90534c07f1985899973 (diff)
downloadgn-docs-d029d5d7f8ead1f1de8d318045004a4a6f68f5fb.tar.gz
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+<p>The Affymetrix Genechip Mouse Clariom S was used to examine gene expression (Affymetrix, California, United States). Two hundred nanograms of DNased total RNA was amplified, labeled, and fragmented using Ambion Whole Transcript (WT) Expression Kit according to manufacturer&rsquo;s protocol (Thermo Fisher Scientific, Santa Clara, California United States). Briefly, samples are hybridized overnight according to manufacturer&rsquo;s protocols; samples are then washed and stained on Affymetrix GeneChip Fluidics Station 450 (Affymetrix, California, United States). Samples were then scanned using the GeneChip Scanner 3000 (Applied Biosystems, California, United States).&nbsp; Data was normalized and analyzed for quality control in Affymetrix Expression Console Software using RMA-sketch normalization (Affymetrix, California, United States). After normalization and quality control, a total number of 22,203 probe sets were used for subsequent data analysis. A total of 128 samples were used&mdash;4 samples per treatment (control, ethanol), sex (male, female), and strain (B6, D2, BXD2, BXD48a, BXD60, BXD71, BXD73, BXD100).</p>