From: Charles Plessy Date: Thu, 20 Jan 2011 13:49:59 +0000 (+0900) Subject: # Addition and correction. X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=1b77ca9e9f9038c560fe8aeb3a2601cb35cde24e;p=source.git # Addition and correction. --- diff --git a/biblio/18477713.mdwn b/biblio/18477713.mdwn index ea423737..6a0f6522 100644 --- a/biblio/18477713.mdwn +++ b/biblio/18477713.mdwn @@ -1,3 +1,3 @@ [[!meta title="A high-resolution, nucleosome position map of C. elegans reveals a lack of universal sequence-dictated positioning."]] [[!tag not_read sequencing]] -[[!pmid 18477713 desc="Contains a descriptioni of equencing by oligonucleotide ligation and detection (SOLiD)."]] +[[!pmid 18477713 desc="Contains a description of sequencing by oligonucleotide ligation and detection (SOLiD)."]] diff --git a/biblio/19213877.mdwn b/biblio/19213877.mdwn index 2a6f338e..ba7f58ba 100644 --- a/biblio/19213877.mdwn +++ b/biblio/19213877.mdwn @@ -1,3 +1,3 @@ [[!meta title="Genome-Wide Analysis In Vivo of Translation with Nucleotide Resolution Using Ribosome Profiling."]] [[!tag sequence_tags method]] -[[!pmid 19213877 desc="Also detects the small “upstream open reading frames” (uORFs). Uses circularisation by ssDNA ligase to avoid the bias of the RNA ligase classicaly used to clone small RNAs."]] +[[!pmid 19213877 desc="Also detects the small “upstream open reading frames” (uORFs). Uses circularisation by ssDNA ligase to avoid the bias of the RNA ligase classicaly used to clone small RNAs. The cDNAs are then linearised with APE1 (human apurinic/apyrimidinic (AP) endonuclease), before bridge PCR."]]