Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
Google News,
Main The transfer of genes from cytoplasmic organelles to the cell nucleus underpins the endosymbiotic theory of the origin of…
Main The transfer of genes from cytoplasmic organelles to the cell nucleus underpins the endosymbiotic theory of the origin of…
Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome — the DNA inherited from your…
Genetic mutations can be benign or cancerous – a new method to differentiate between them could lead to better treatments…
Scientists can now readily read cell DNA to identify mutations. Andrii Yalanskyi/iStock via Plus Scientists can now readily…
Using data to identify the genetic changes that cause healthy cells to become malignant can help doctors select therapies that…
Calvo, S. E.
One cancer-driving mutation can lead to a cascade of other mutations that lead to uncontrollable cell division.
Tumors contain thousands of genetic changes, but only a few are actually cancer-causing.
One cancer-driving mutation can lead to a cascade of other mutations that lead to uncontrollable cell division.
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome – the DNA inherited from your…
Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome - the DNA inherited from your…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(THE CONVERSATION) Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome – the DNA…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Ryan Layer…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome – the DNA inherited from your…
Identifying the difference between normal genetic variation and disease-causing mutations can sometimes be difficult.
Most of the roughly 40 trillion cells of your body have nearly identical copies of your genome – the DNA inherited from your…
The first draft of the human genome was published 20 years ago in 2001, took nearly three years, and cost between $500 million…
A complete human genome, seen here in pairs of chromosomes, offers a wealth of information, but it is hard connect genetics to…
Courtesy of Xavier Bofill De Ros, National Institutes of Health The first draft of the human genome was published 20 years ago…
By Xavier Bofill De Ros Apr 16, 2021 The first draft of the human genome was published 20 years ago in 2001, took nearly three…
The first draft of the human genome was published 20 years ago in 2001, took nearly three years and cost between US$500 million…
– By Xavier Bofill De Ros, Research Fellow in RNA biology, National Institutes of Health The first draft of the human genome…
The first draft of the human genome was published 20 years ago in 2001, took nearly three years and cost between US$500 million…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) The first…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) Xavier Bofill…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
The first draft of the human genome was published 20 years ago in 2001, took nearly three years and cost between US$500 million…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(The Conversation is an independent and nonprofit source of news, analysis and commentary from academic experts.) (THE…
(THE CONVERSATION) The first draft of the human genome was published 20 years ago in 2001, took nearly three years and cost…
When the first complete sequence of the human genome was published in 2003, the Human Genome Project leader, Francis Collins…
When the first complete sequence of the human genome was published in 2003, the Human Genome Project leader, Francis Collins…
Illustration by the project twins When geneticist Daniel MacArthur checks into his lab, the first thing he does is fire up Slack…
För femte gången listar Dagens Medicin årets tio främsta forskningsnyheter. 2016 toppas listan av en efterlängtad nyhet inom…
The ExAC database has shown that many mutations thought to be harmful are benign.
Some genetic mutations that have been thought to be harmful are turning out to be innocuous, Nature News reports.
One of the major findings of the Exome Aggregation Consortium (ExAC), the largest-ever catalogue of genetic variation in the…
Genomics-the study of all the genetic instructions in an organism - can help researchers develop new diagnostic tools, tailor…
Genomics-the study of all the genetic instructions in an organism – can help researchers develop new diagnostic tools, tailor…
杂志英拜生物(生物谷) · 2016-08-30 16:03 8月份即将结束,本月Nature杂志又有哪些亮点研究值得学习呢?小编对此进行了整理,与各位一起学习。 【1】致癌克隆动力学研究 doi | 10.1038/nature19069 本文对从初始癌化…
엑솜 집합체 컨소시엄(Exome Aggregation Consortium, ExAC) 프로젝트의 일부분으로써, Daniel MacArthur와 공동연구원들은 질환이 있었던 조상을 가진 약 60,706명의 개인으로부터 얻어진 고해상도…
Using a massive exome sequencing database, researchers have identified millions of genetic variants for further study.
Aug 22, 2016 06:33 AM EDT Finns are now genetically considered an independent population instead of a part of the European…
Aug 22, 2016 06:33 AM EDT Finns are now genetically considered an independent population instead of a part of the European…
Researchers have published the first analysis of the 60,000 people sequenced through the Exome Aggregation Consortium (ExAC).
Perjantai 19.8.2016 klo 21.39 Suomalaisilla on esimerkiksi diabetekselle altistava geenimuutos, jota ei ole missn muualla…
Suomalaisten geeniperimä eroaa eurooppalaisista niin paljon, että heidät pitää luokitella omaksi väestökseen.
Laaja geenitutkimus todistaa suomalaiset omalaatuisiksi: Eurooppalaiset pitäisi jakaa suomalaisiksi ja ei-suomalaisiksi…
Research led by Dr Monkol Lek of the University of Sydney and Dr Daniel MacArthur of The Broad Institute of MIT and Harvard…
Delar av den genetiska koden har blivit kartlagd hos 60 000 människor. Foto: Johntisza CC BY 20 Nu kommer en första analys av…
NEW YORK (GenomeWeb) – Members of the Exome Aggregation Consortium led by scientists at the Broad Institute of MIT and Harvard…
参与人类外显子组整合数据库(ExAC)项目的Daniel MacArthur及同事生成并分析了来自60,706位被试者的高质量外显子组测序数据,这些被试者来自于不同的地理人口系谱。这一研究是迄今为止对人类蛋白编码遗传变异最为全面的记录,对于低频蛋白编码变体的…
”Suomalaiset” ja ”ei-suomalaiset”. Näihin kahteen ryhmään jaetaan eurooppalaiset tuoreessa Nature-tiedejulkaisussa ilmestyneessä…
Actualizado el 18 de agosto de 2016 a las 10:43 am Nueva York Un enorme catálogo de ADN humano está ayudando a científicos a…
De nya resultaten väcker frågor om hur bra vår kunskap är gällande genetiska variationer.
Researchers associated with the Exome Aggregation Consortium (ExAC) have catalogued and released the gene sequencing data of…
/ no comments Published in today’s book of Nature, a investigate led by Dr Monkol Lek of a University of Sydney and Dr Daniel…
Large-scale reference data sets of human genetic variation are critical for the medical and functional interpretation of DNA…
at 5:06 AM Published in today's edition of Nature, the research led by Dr Monkol Lek of the University of Sydney and Dr Daniel…
PUBLICADO EN 'NATURE' JANO.es · 18 agosto 2016 10:04 El proyecto The Exome Aggregation Consortium, que cuenta con la participació…
Suomalaisten geeniperimä eroaa eurooppalaisista niin paljon, että heidät pitää luokitella omaksi väestökseen.
Published in today's edition of Nature, the research led by Dr Monkol Lek of the University of Sydney and Dr Daniel MacArthur…
Published in today's edition of Nature, the research led by Dr Monkol Lek of the University of Sydney and Dr Daniel MacArthur…
FLICKR, SHAURY NASH An international team led by researchers at the Broad Institute of MIT and Harvard has compiled and…
参与人类外显子组整合数据库(ExAC)项目的Daniel MacArthur及同事生成并分析了来自60,706位被试者的高质量外显子组测序数据,这些被试者来自于不同的地理人口系谱。这一研究是迄今为止对人类蛋白编码遗传变异最为全面的记录,对于低频蛋白编码变体的…
엑솜 집합체 컨소시엄(Exome Aggregation Consortium, ExAC) 프로젝트의 일부분으로써, Daniel MacArthur와 공동연구원들은 질환이 있었던 조상을 가진 약 60,706명의 개인으로부터 얻어진 고해상도…
Published in today's edition of Nature, the research led by Dr Monkol Lek of the University of Sydney and Dr Daniel MacArthur…
Published in today's edition of Nature, the research led by Dr Monkol Lek of the University of Sydney and Dr Daniel MacArthur…
The largest study of its kind into type 2 diabetes has produced the most detailed picture to date of the genetics underlying…