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+[[!meta title="A new strategy to amplify degraded RNA from small tissue samples for microarray studies."]]
+[[!tag reverse_transcription amplification]]
+
+Xiang CC, Chen M, Ma L, Phan QN, Inman JM, Kozhich OA, Brownstein MJ.
+
+Nucleic Acids Res. 2003 May 1;31(9):e53. doi:10.1093/nar/gng053
+
+A new strategy to amplify degraded RNA from small tissue samples for microarray studies.
+
+[[!pmid 12711698 desc="Uses T3N9 instead of T7dT during all the RT reactions. No 3' bias. Efficient on degraded RNA. Independant of polyadenylation (useful for non-polyA genes, like histones)."]]

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@@ -20,12 +20,6 @@ Aminoallyl UTP to labal cRNAs. In contrast to cDNAs, DMSO is required for subseq
 12161654 [misc]
 Fluorescent bar-coded oligos to monitor transcription in vivo.
 
-10499525 [single cell]
-Single cell RT-PCR.
-
-12711698 [amplification] [tracked]
-Uses T3N9 instead of T7dT during all the RT reactions. No 3' bias. Efficient on degraded RNA. Independant of polyadenylation (useful for non-polyA genes, like histones).
-
 14606961 [libraries]
 The nuclease activity of T7 RNA pol could also show some transcript specificity.