Add keyword.

diff --git a/biblio/29434199.mdwn b/biblio/29434199.mdwn
index 46e40f05c8b90e148847a38c00e906c90eaccd7a..2dd301e03fb6c74302d3e767edfaabec6322c151 100644 (file)
--- a/biblio/29434199.mdwn
+++ b/biblio/29434199.mdwn
@@ -7,4 +7,4 @@ Hayashi T, Ozaki H, Sasagawa Y, Umeda M, Danno H, Nikaido I.
 
 Single-cell full-length total RNA sequencing uncovers dynamics of recursive splicing and enhancer RNAs.
 
-[[!pmid 29434199 desc="First-strand cDNAs are synthesised with a RNAse H minus reverse-transcriptase.  DNAse I introduces nicks that prime synthesis of new cDNA molecules.  T4gp32 promotes the strand-displacement activity of the reverse-transcriptase.  Second-strand cDNAs are synthethised with Klenow fragment (3′ → 5′ exo-) primed with NSRs.  In single cells, genomic DNA needs to be removed because of the DNAseI digestion during RT and the low-complexity priming of the second-strand synthesis with NSRs.  The resulting DNA molecules are tagmented and sequenced with standard methods.  Thus, the method is non-stranded.  Despite the use of NSRs, the rRNA rate stays between 20 and 30 %."]]
+[[!pmid 29434199 desc="RamDA-seq.  First-strand cDNAs are synthesised with a RNAse H minus reverse-transcriptase.  DNAse I introduces nicks that prime synthesis of new cDNA molecules.  T4gp32 promotes the strand-displacement activity of the reverse-transcriptase.  Second-strand cDNAs are synthethised with Klenow fragment (3′ → 5′ exo-) primed with NSRs.  In single cells, genomic DNA needs to be removed because of the DNAseI digestion during RT and the low-complexity priming of the second-strand synthesis with NSRs.  The resulting DNA molecules are tagmented and sequenced with standard methods.  Thus, the method is non-stranded.  Despite the use of NSRs, the rRNA rate stays between 20 and 30 %."]]