From: Charles Plessy <https://launchpad.net/~plessy>
Date: Thu, 10 Feb 2011 06:33:53 +0000 (+0900)
Subject:  # Transfert.
X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=f819fe9837b9ed63883bb12c598a1308a2b35ad0;p=source%2F.git

 # Transfert.
---

diff --git a/biblio/10037822.mdwn b/biblio/10037822.mdwn
index 222e5c0c..1b4f93be 100644
--- a/biblio/10037822.mdwn
+++ b/biblio/10037822.mdwn
@@ -1,3 +1,3 @@
 [[!meta title="Amplification of cDNA ends based on template-switching effect and step-out PCR."]]
-[[!tag amplification]]
-[[!pmid 10037822 desc="Uses PCR-Suppression effect to limit background in 5'RACE, due to "non specific" template switching."]]
+[[!tag template_switching PCR method ]]
+[[!pmid 10037822 desc="To counter template-switching happening from inside the oligonucleotide instead of its tail."]]
diff --git a/biblio/To_Do b/biblio/To_Do
index 5abd200b..a8fddf41 100644
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -729,9 +729,6 @@ Suppressive PCR allows the use of one gene-specific primer, and one random prime
 16049110 [enhancers]
 The minimal promoter used here is from GATA2 and may cause a bias towards enhancers of developmental regulators.
 
-10037822 [libraries]
-To counter internal template swiching.
-
 16179648 [enhancers]
 Neighbour genes of clusters of NCECR are enriched in Transcription Factor ontologies. 16 NCECR were experimentally investigated (10/16 are positive), but the gene names are not given.