I recently returned, albeit part-time, to work in academia and I was offered the chance to teach. Many academics in scientific research never teach, other than perhaps one-to-one “teaching” of a new doctoral student. In the past, I have presented my work to other scientists and also given a few guest lectures to undergraduates; しかし [...]
Author Archives: ポールデニー
Applications & Bottlenecks In Next Generation Sequencing, Day 2
This word cloud shows the words that people used in the ice-breaking session, that I mentioned in my last post, to describe what they hoped to gain from the conference. On Day 2, our Keynote speaker was: Dr Anneke Seller, Oxford Genetics: Clinical utility; actionable #NGS diagnosis for patients & families http://t.co/0mmrSx1Dd5 #ngsmanchester — Paul [...]
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Applications & Bottlenecks In Next Generation Sequencing
After months of preparation and the occasional sleepless night, November 5th arrived. It wasn’t only Bonfire Night, but also the beginning of a two-day conference, focusing on NGS in clinical genetics laboratories. Organised by my colleagues and friends from biotexcel and myself, it was held in the Manchester Conference Centre, で, naturally enough, Manchester, 英国. In order to break [...]
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そう, What Do Your Genes DO?
Genes are not passive. They are the target of molecular “dimmer switches”; typically (but not always) specific proteins, which dial up or turn down their activity. Most genes are translated into proteins, but discovering the true role of those proteins, in the life of a cell or a whole organism, is still one of the great challenges [...]
Posted in 疾患モデル, ゲノミクス, ターゲット発見
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我々の遺伝子の一部が不足しています…しかしどれ?
One can think of genes in a number of ways: DNAレベルで – 単にヌクレオチドの直鎖状配列として, ONE一定の順序で, で “ノーマル” 状態, or Again as a DNA molecule, 生物のそれを覚えている遺伝子, むしろ試験管中のDNAの断片に比べ, are subject [...]
Posted in 疾患モデル, ゲノミクス
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Genetics Society Spring Meeting: Genomics for Health and Society
The aim of of the meeting was to begin to answer the question: “What will be the impact of large-scale sequencing of human populations in the 21st Century?” Held at The Royal Society in London on 19th April 2013, the meeting brought together some distinguished figures from clinical genetics, population genomics, DNA fingerprinting and the [...]
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Gene & Cell Therapy For the People
The Annual meeting of the British Society for Gene and Cell Therapy, as well as being aimed at the expert, included a day of presentations intended for students and the public. Aimed primarily at GCSE and A-level students, but open to all, this one day interactive event provided an opportunity to discuss and debate gene and [...]
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クリニックに次世代シーケンシングの移動, 一部 2
first attempt at live tweets from #ngs2013 http://t.co/SbWrGx8weI — ポールデニー (@pauldennyuk) 3月 12, 2013 In my last post, I summarised the first four talks from this symposium: 1st Oxford Workshop and Symposium, 4th Techgene Knowledge Network Meeting, “NGS2013 Next generation Sequencing: Bioinformatics and Data Analysis” You could also read the Tweets from the meeting [...]
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クリニックに次世代シーケンシングの移動
栄光の日に (しかし、北極のような風と!) 今週これまでに, 私は診断遺伝学クリニックで悪用NGSに関するシンポジウムに出席: Off to # Ngs2013 today at Wolfson College Oxford http://t.co/SbWrGx8weI #NGS #Clinical #Dx #diagnostic #personalisedmed Should be good — ポールデニー (@pauldennyuk) 3月 12, 2013 スピーカーは臨床医だった, bioinformaticians and biomedical [...]
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どんな小さなマウスはヒトの先天異常についての私達に教えるかもしれません?
Mice are born with their eyes tightly shut, わずか数日後に最初の時間のためにそれらを開く. So when a mouse was noticed that was smaller than normal and had been born with it’s eyes open, それが注目を集めました. このような異常はすべての動物施設で自然発生する, but sometimes they are not [...]
Posted in 疾患モデル
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