Publication date
October 2013
DOI Publisher
Springer Science and Business Media LLC Journal
Genome MedicineAbstract
A report on the Genomic Disorders 2012: Genomics of Rare Diseases meeting, Hinxton, UK, 21-23 March 2012
A report on the Genomic Disorders 2012: Genomics of Rare Diseases meeting, Hinxton, UK, 21-23 March 2012
Whole-exome/whole-genome sequencing (WES/WGS) has the potential to enhance genetic diagnosis of rare...
Genomics is a complex field that is taking an increasing role in many aspects of healthcare. Genomic...
Genomics medicine and molecular genetics are experiencing a surge of interest as well as a push for ...
A report on the Keystone Symposium 'Cancer Genomics and Epigenomics', Taos, USA, 19-24 February 2008
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
High-throughput sequencing technologies have changed the way we identify, study and understand the r...
BACKGROUND: Human genome sequencing has transformed our understanding of genomic variation and its r...
BACKGROUND: Human genome sequencing has transformed our understanding of genomic variation and its r...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
After a long and largely disappointing detour, Genome Research has reidentified Rare Diseases as a m...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
SummaryBackgroundHuman genome sequencing has transformed our understanding of genomic variation and ...
A report on the Keystone Symposium 'Biological Discovery Using Diverse High-Throughput Data', Steamb...
Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic...
Whole-exome/whole-genome sequencing (WES/WGS) has the potential to enhance genetic diagnosis of rare...
Genomics is a complex field that is taking an increasing role in many aspects of healthcare. Genomic...
Genomics medicine and molecular genetics are experiencing a surge of interest as well as a push for ...
A report on the Keystone Symposium 'Cancer Genomics and Epigenomics', Taos, USA, 19-24 February 2008
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
High-throughput sequencing technologies have changed the way we identify, study and understand the r...
BACKGROUND: Human genome sequencing has transformed our understanding of genomic variation and its r...
BACKGROUND: Human genome sequencing has transformed our understanding of genomic variation and its r...
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licen...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
After a long and largely disappointing detour, Genome Research has reidentified Rare Diseases as a m...
Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing...
SummaryBackgroundHuman genome sequencing has transformed our understanding of genomic variation and ...
A report on the Keystone Symposium 'Biological Discovery Using Diverse High-Throughput Data', Steamb...
Genetic Analysis Workshop 17 (GAW17) provided a platform for evaluating existing statistical genetic...
Whole-exome/whole-genome sequencing (WES/WGS) has the potential to enhance genetic diagnosis of rare...
Genomics is a complex field that is taking an increasing role in many aspects of healthcare. Genomic...
Genomics medicine and molecular genetics are experiencing a surge of interest as well as a push for ...
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