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"Project-Id-Version: PACKAGE VERSION\n"
-"POT-Creation-Date: 2020-11-02 03:50+0000\n"
+"POT-Creation-Date: 2020-11-02 06:36+0000\n"
"PO-Revision-Date: YEAR-MO-DA HO:MI+ZONE\n"
"Last-Translator: FULL NAME <EMAIL@ADDRESS>\n"
"Language-Team: LANGUAGE <LL@li.org>\n"
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"I have complemented my work on CAGE with the development of a gene-centred "
-"technique for detecting promoters, termed Deep-RACE ([Olivarius and coll., "
-"2009](https://pubmed.gov/19317658), [Plessy and coll., 2012](http://dx.doi."
-"org/10.1002/9783527644582.ch4)), which we used to validate our discovery of "
-"the pervasive expression of retrotransposons detected by CAGE ([Faulkner and "
-"coll., 2009](https://pubmed.gov/19377475)). To study transcription start "
-"activity at nucleotide resolution in zebrafish transfected with chimeric "
-"transgenes containing a copy of an endogenous promoter, I combined Deep-"
-"RACE, CAGE and paired-end sequencing in a technology that we called “Single-"
-"Locus CAGE” ([Haberle and coll., 2014](https://pubmed.gov/24531765)). With "
-"my contributions related to CAGE development and analysis, I have been a "
-"**member of the FANTOM consortium** since FANTOM3."
+"technique for detecting promoters, termed **Deep-RACE** ([Olivarius and "
+"coll., 2009](https://pubmed.gov/19317658), [Plessy and coll., 2012](http://"
+"dx.doi.org/10.1002/9783527644582.ch4)), which we used to validate our "
+"discovery of the pervasive expression of retrotransposons detected by CAGE "
+"([Faulkner and coll., 2009](https://pubmed.gov/19377475)). To study "
+"transcription start activity at nucleotide resolution in zebrafish "
+"transfected with chimeric transgenes containing a copy of an endogenous "
+"promoter, I combined Deep-RACE, CAGE and paired-end sequencing in a "
+"technology that we called “Single-Locus CAGE” ([Haberle and coll., 2014]"
+"(https://pubmed.gov/24531765)). With my contributions related to CAGE "
+"development and analysis, I have been a **member of the FANTOM consortium** "
+"since FANTOM3."
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"(https://pubmed.gov/24904046)), 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. I also applied the nanoCAGE technology to patient "
-"samples infected with the human papillomavirus (HPV) ([Taguchi and coll., "
-"2020](https://pubmed.gov/33093512))."
+"**T cell antigen receptors**. I also applied the nanoCAGE technology to "
+"patient samples infected with the **human papillomavirus** (HPV) ([Taguchi "
+"and coll., 2020](https://pubmed.gov/33093512))."
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"I joined OIST in 2018, to study **the genetic structure and population "
-"variations** of an animal plankton, _Oikopleura dioica_, that has a genome "
-"50 time more compact than the human one, which empowers us to sequence at "
-"chromosomal resolution many individual sampled from all over the World."
+"variations** of an animal plankton, **_Oikopleura dioica_**, that has a "
+"genome 50 time more compact than the human one, which empowers us to "
+"sequence at chromosomal resolution many individual sampled from all over the "
+"World. Its mitochondria use a different genetic code than ours ([Pichon and "
+"coll., 2019](https://pubmed.gov/32148763)). We assembled whole-chromosome "
+"sequences for the Okinawan _O. dioica_ population ([Bliznina and coll., 2020]"
+"(https://doi.org/10.1101/2020.09.11.292656)), which has 3 pairs of "
+"chromosomes ([Liu and coll, 2020](https://f1000research.com/articles/9-780/"
+"v1)) like the other dioceous species."
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