From: Charles Plessy <plessy@riken.jp>
Date: Wed, 6 Sep 2017 06:10:45 +0000 (+0900)
Subject: Old.
X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=8beee495065db9a43ba86a023822b8c46c31050b;p=source%2F.git

Old.
---

diff --git a/biblio/2020554.mdwn b/biblio/2020554.mdwn
new file mode 100644
index 00000000..f11b3ad5
--- /dev/null
+++ b/biblio/2020554.mdwn
@@ -0,0 +1,10 @@
+[[!meta title="A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors."]]
+[[!tag libraries]]
+
+Nucleic Acids Res. 1991 Mar 11;19(5):1156 doi:10.1093/nar/19.5.1156
+
+Holton TA1, Graham MW.
+
+A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors.
+
+[[!pmid 2020554 desc="Tails open plasmid with ddT using terminal transferase."]]
diff --git a/biblio/To_Do b/biblio/To_Do
index ac58d916..2b3e18b4 100644
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -686,9 +686,6 @@ Different collaboration network in different research consortiums.
 16120967 [enzymes]
 Apparently, only one of the two head-to-head sites is cut...
 
-2020554 [libraries]
-Uses terminal transferase.
-
 16046619 [mining]
 When a group of TFs have more than one Transfac entry, only the most over-represented is taken into account to build the network.