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+[[!meta title="Microfluidic devices for high-throughput gene expression profiling of single hESC-derived neural stem cells."]]
+[[!tag single_cell beads microfluidic reverse_transcription]]
+
+Chen Y, Zhong JF.
+
+Methods Mol Biol. 2008;438:293-303. doi:10.1007/978-1-59745-133-8_22
+
+Microfluidic devices for high-throughput gene expression profiling of single hESC-derived neural stem cells.
+
+[[!pmid 18369765 desc="Another implementation of reverse-transcription on beads"]]

diff --git a/biblio/To_Do b/biblio/To_Do
index 01f580ae306685c81760b0e59a5931677ab3e463..838ec06e187fb4de5906932418d8e838b7733202 100644 (file)
--- a/biblio/To_Do
+++ b/biblio/To_Do
@@ -566,9 +566,6 @@ Degrades single-strand DNA, not RNA nor double strand DNA.
 16964207 [misc]
 Reommends to use only dbSNP entries which have a phred score higher than 40.
 
-15693942 [mining]
-Uses a highly replicated experimental desigh to show that metabolic genes vary in their expresison between tissues, individuals and populations.
-
 16698958 [enhancers]
 Defines the concept of "maximal N-mers".
 
@@ -791,12 +788,6 @@ Did not find FANTOM3 CAGE tags.
 17412960 [qtl]
 First analysis within a breed, then second analysis comparing small and giant breeds.
 
-16105897 [mining]
-Two genes of opposite expression profiles define a "top scoring pair", and are used to sort the other genes.
-
-18369765 [microfluidics]
-Another implementation of the revese-transcription on beads.
-
 18417536 [enhancers]
 First report of a conserved enhancer in a coding sequence ?