From: admin Date: Mon, 15 Jun 2020 07:45:33 +0000 (+0000) Subject: updated PO files X-Git-Url: https://source.charles.plessy.org/?a=commitdiff_plain;h=64fc8fa37674d8704327823aa5fd9f75ade7fb98;p=source.git updated PO files --- diff --git a/open-source-biologist.en.po b/open-source-biologist.en.po index 9a9a3dce..16ff1771 100644 --- a/open-source-biologist.en.po +++ b/open-source-biologist.en.po @@ -7,7 +7,7 @@ msgid "" msgstr "" "Project-Id-Version: PACKAGE VERSION\n" -"POT-Creation-Date: 2020-06-15 07:41+0000\n" +"POT-Creation-Date: 2020-06-15 07:45+0000\n" "PO-Revision-Date: YEAR-MO-DA HO:MI+ZONE\n" "Last-Translator: FULL NAME \n" "Language-Team: LANGUAGE \n" @@ -16,16 +16,21 @@ msgstr "" "Content-Type: text/plain; charset=UTF-8\n" "Content-Transfer-Encoding: 8bit\n" +#. type: Title - +#, no-wrap +msgid "Charles Plessy, open-source biologist" +msgstr "" + #. type: Plain text msgid "" "My training as a researcher started with developmental genetics in " "drosophila and zebrafish, where I studied the activity of transcription " -"enhancers (Blader et al., 2003) and their evolutionary conservation (Plessy " -"et al., 2005). This gave me a strong interest for whole-transcriptome " -"analysis and technology. For that purpose, I have joined RIKEN in 2004, " -"where have worked on high-throughput methods for profiling promoters and " -"inferring gene networks, and in particular on CAGE (Cap Analysis Gene " -"Expression)." +"enhancers ([Blader and coll., 2003](https://pubmed.gov/12559493)) and their " +"evolutionary conservation (Plessy et al., 2005). This gave me a strong " +"interest for whole-transcriptome analysis and technology. For that purpose, " +"I have joined RIKEN in 2004, where have worked on high-throughput methods " +"for profiling promoters and inferring gene networks, and in particular on " +"CAGE (Cap Analysis Gene Expression)." msgstr "" #. type: Plain text @@ -39,8 +44,8 @@ msgid "" "molecular barcodes (Tang et al., 2013), combining multiple cap-enrichment " "steps (Batut et al., 2013), benchmarking the use of locked nucleic acids for " "template switching (Harbers et al., 2013), and reducing the number of primer " -"artefacts and unwanted sequences generated by ribosomal RNAs using " -"low-complexity “pseudo-random” reverse-transcription primers (Arnaud et al., " +"artefacts and unwanted sequences generated by ribosomal RNAs using low-" +"complexity “pseudo-random” reverse-transcription primers (Arnaud et al., " "2016)." msgstr "" @@ -78,10 +83,10 @@ msgid "" "neuroscience, I have applied nanoCAGE to the study of single neuron cell " "types, for instance the olfactory neurons (Plessy et al., 2012), or in " "dopaminergic cells, where we could demonstrate the expression of haemoglobin " -"in the midbrain (Biagioli et al., 2009). We are also exploring the " -"sub-cellular localisation of RNA in Purkinje neurons (Kratz et al., 2014), " -"and neurogenesis in the mouse olfactory epithelium using single-cell CAGE " -"and ATAC-seq techniques. In parallel with this promoter-centric work, I have " +"in the midbrain (Biagioli et al., 2009). We are also exploring the sub-" +"cellular localisation of RNA in Purkinje neurons (Kratz et al., 2014), and " +"neurogenesis in the mouse olfactory epithelium using single-cell CAGE and " +"ATAC-seq techniques. In parallel with this promoter-centric work, I have " "also explored the huge repertoire of the T cell antigen receptors." msgstr ""