From: Charles Plessy <plessy@riken.jp>
Date: Thu, 24 Aug 2017 00:35:35 +0000 (+0900)
Subject: Vieux.
X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=3d35e8fc5a13c03883e5c3d6af1ea8b720a08b0b;p=source%2F.git

Vieux.
---

diff --git a/biblio/11768647.mdwn b/biblio/11768647.mdwn
new file mode 100644
index 00000000..c012fdef
--- /dev/null
+++ b/biblio/11768647.mdwn
@@ -0,0 +1,10 @@
+[[!meta title="Serial analysis of gene expression in a single cell."]]
+[[!tag sequence_tags single_cell]]
+
+Schober MS, Min YN, Chen YQ.
+
+Biotechniques. 2001 Dec;31(6):1240-2.
+
+Serial analysis of gene expression in a single cell.
+
+[[!pmid 11768647 desc="Lysis in Dynabeads buffer, followed by first strand synthesis from poly-A."]]
diff --git a/biblio/9742245.mdwn b/biblio/9742245.mdwn
new file mode 100644
index 00000000..c302e665
--- /dev/null
+++ b/biblio/9742245.mdwn
@@ -0,0 +1,10 @@
+[[!meta title="Expression profiling of single cells using 3 prime end amplification (TPEA) PCR."]]
+[[!tag single_cell]]
+
+Dixon AK, Richardson PJ, Lee K, Carter NP, Freeman TC.
+
+Nucleic Acids Res. 1998 Oct 1;26(19):4426-31.
+
+Expression profiling of single cells using 3 prime end amplification (TPEA) PCR.
+
+[[!pmid 9742245 desc="Nucleus removed by spinning. 1st PCR with poly-T and random primer. 2nd PCR nested and gene specific."]]
diff --git a/biblio/To_Do b/biblio/To_Do
index 6698258d..c9e05000 100644
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -153,9 +153,6 @@ Engeneered T7 used to generate dye-terminated amplification products.
 15271495 [single cell]
 Review
 
-9742245 [single cell] [tracked]
-Nucleus removed by spinning. 1st PCR with poly-T and random primer. 2nd PCR nested and gene specific.
-
 15070753 [libraries]
 Library of DNAseI ends, to map hypersensitive sites. Substrraction with a HS-depleted tester.
 
@@ -335,9 +332,6 @@ Alternative promoters which transcribe variants with different translational eff
 14663149 [libraries] [tracked]
 5' 20mers to map transcription start sites, and mesaure their usage.
 
-11768647 [single cell]
-Lysis in Dynabeads buffer, followed by first strand synthesis from poly-A.
-
 15342556 [genome]
 These blocks contain most validated and predicted transcription factor binding sites.