From: Charles Plessy <plessy@riken.jp>
Date: Tue, 7 Nov 2017 07:56:53 +0000 (+0900)
Subject: Old
X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=a0d5021b15432f2969f8e6c598f1dd58abc6687f;p=source.git

Old
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diff --git a/biblio/12613261.mdwn b/biblio/12613261.mdwn
new file mode 100644
index 00000000..16d86772
--- /dev/null
+++ b/biblio/12613261.mdwn
@@ -0,0 +1,10 @@
+[[!meta title="Probe generation directly from small numbers of cells for DNA microarray studies."]]
+[[!tag random_priming amplification]]
+
+Biotechniques. 2003 Feb;34(2):386-8, 390, 392-3
+
+Xiang CC, Chen M, Kozhich OA, Phan QN, Inman JM, Chen Y, Brownstein MJ.
+
+Probe generation directly from small numbers of cells for DNA microarray studies.
+
+[[!pmid 12613261 desc="Uses T3N9 random nonamer amplification rounds (up to 5), after an initial T7dT RT."]]
diff --git a/biblio/To_Do b/biblio/To_Do
index e246214c..9f82fcfd 100644
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -41,9 +41,6 @@ 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.
 
-12613261 [amplification]
-Uses T3N9 random nonamer amplification rounds (up to 5), after an initial T7dT RT.
-
 10499525 [single cell]
 Single cell RT-PCR.