Add to ORKGn whole-genome sequencing “I suggest herein that the genomics research community replace the term ‘incidental findings ’ with the term ‘unrelated findings’, given that there is nothing incidental about proving causality for any mutation.
For almost 15 years, genome research has focused on the search for major risk factors in common dise...
The editorial (1) on CEBP publication criteria is timely and important. However, the days when most ...
How genomics is changing our view of cancer Cancer knows no boundaries, it may be the only true non-...
To the Editor: Yang et al. (Oct. 17 issue)(1) report the application of whole-exome sequencing in 25...
sued the department of clinical diagnosis in Lydon, the XBG mutation database, and the journal Human...
Correction to this paper has been published: https://doi.org/10.1038/s41467-020-20128-w
An amendment to this paper has been published and can be accessed via a link at the top of the paper
A recent announcement from Oregon Health & Science University stated that their scientists have elim...
Whole-genome sequencing (WGS) is revolutionizing medical research and has the potential to serve as ...
Correction to this paper has been published: https://doi.org/10.1038/s41467-020-20128-w
Next-generation sequencing is radically changing how DNA diagnostic laboratories operate. What start...
In 2013, the American College of Medical Genetics (ACMG) examined the issue of incidental findings i...
nipulation, biochemical and molecular experimentation, and the availability of its full genomic sequ...
Erratum in Corrigendum. [Expert Rev Mol Diagn. 2016]International audienceNon-targeted identifica...
Cancer is underlined by genetic changes. In an unprecedented international effort, the Pan-Cancer An...
For almost 15 years, genome research has focused on the search for major risk factors in common dise...
The editorial (1) on CEBP publication criteria is timely and important. However, the days when most ...
How genomics is changing our view of cancer Cancer knows no boundaries, it may be the only true non-...
To the Editor: Yang et al. (Oct. 17 issue)(1) report the application of whole-exome sequencing in 25...
sued the department of clinical diagnosis in Lydon, the XBG mutation database, and the journal Human...
Correction to this paper has been published: https://doi.org/10.1038/s41467-020-20128-w
An amendment to this paper has been published and can be accessed via a link at the top of the paper
A recent announcement from Oregon Health & Science University stated that their scientists have elim...
Whole-genome sequencing (WGS) is revolutionizing medical research and has the potential to serve as ...
Correction to this paper has been published: https://doi.org/10.1038/s41467-020-20128-w
Next-generation sequencing is radically changing how DNA diagnostic laboratories operate. What start...
In 2013, the American College of Medical Genetics (ACMG) examined the issue of incidental findings i...
nipulation, biochemical and molecular experimentation, and the availability of its full genomic sequ...
Erratum in Corrigendum. [Expert Rev Mol Diagn. 2016]International audienceNon-targeted identifica...
Cancer is underlined by genetic changes. In an unprecedented international effort, the Pan-Cancer An...
For almost 15 years, genome research has focused on the search for major risk factors in common dise...
The editorial (1) on CEBP publication criteria is timely and important. However, the days when most ...
How genomics is changing our view of cancer Cancer knows no boundaries, it may be the only true non-...