From: Charles Plessy <plessy@riken.jp>
Date: Tue, 3 Oct 2017 01:05:13 +0000 (+0900)
Subject: Old
X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=4e3a268244d53424f58fd2588277d61a21be1b56;p=source%2F.git

Old
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diff --git a/biblio/15070753.mdwn b/biblio/15070753.mdwn
new file mode 100644
index 00000000..2e16c75b
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+++ b/biblio/15070753.mdwn
@@ -0,0 +1,10 @@
+[[!meta title="Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries."]]
+[[!tag library epigenetic DNAse-hypersensitivity]]
+
+Sabo PJ, Humbert R, Hawrylycz M, Wallace JC, Dorschner MO, McArthur M, Stamatoyannopoulos JA.
+
+Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4537-42
+
+Genome-wide identification of DNaseI hypersensitive sites using active chromatin sequence libraries.
+
+[[!pmid 15070753 desc="Library of DNAseI ends, to map hypersensitive sites. Substrraction with a HS-depleted tester."]]
diff --git a/biblio/To_Do b/biblio/To_Do
index d16ba759..524dacc7 100644
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -104,9 +104,6 @@ Direct labeling of 10µg total RNA.
 15272081 [libraries]
 81% of the 5'/3' tag pairs could be used to amplify a cDNA by RT-PCR.
 
-14973331 [libraries]
-cDNAs substracted by their former templates. DNS cleaves DNA from DNA/RNA duplexes, leaving RNA molecules intact. This would suggest the strong reduction of abundant transcripts.
-
 8125298 [libraries]
 Oligo capping primary paper.
 
@@ -125,9 +122,6 @@ Engeneered T7 used to generate dye-terminated amplification products.
 15271495 [single cell]
 Review
 
-15070753 [libraries]
-Library of DNAseI ends, to map hypersensitive sites. Substrraction with a HS-depleted tester.
-
 15256515 [genome] [tracked]
 Analysis of the distribution of all possible 8-mers in human proximal promoters. Identifiers 9 clusters of sequence. TATA found only in 2.6% of the promoters.