# Transfert.

diff --git a/biblio/10037822.mdwn b/biblio/10037822.mdwn
index 222e5c0c0dca020ba9ea5ad869d24a84da831aa7..1b4f93be3b1045ae3c26c53d6b8072a35659a724 100644 (file)
--- 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 5abd200b2cd1ed6648c173003a74e53bd2e113c6..a8fddf41d089d4c6d7a28cf66218ae5cf58e1df0 100644 (file)
--- 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.