Rapid methodological advances in statistical and computational genomics have enabled researchers to better identify and interpret both rare and common variants responsible for complex human diseases. As we continue to see an expansion of these advances in the field, it is now imperative for researchers to understand the resources and methodologies available for various data types and study designs. In this review, we provide an overview of recent methods for identifying rare and common variants and understanding their roles in disease etiology. Additionally, we discuss the strategy, challenge, and promise of gene therapy. As computational and statistical approaches continue to improve, we will have an opportunity to translate human genetic ...
Genome and exome sequencing in large cohorts enables characterization of the role of rare variation ...
Novel high-throughput sequencing technologies generate largescale genomic data and are used extensiv...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Rapid methodological advances in statistical and computational genomics have enabled researchers to ...
Collectively, rare genetic disorders affect a substantial portion of the world's population. In most...
Advances in DNA sequencing technology have resulted in the ability to generate genetic data at costs...
Genome sequencing is enabling precision medicine-tailoring treatment to the unique constellation of ...
AbstractThe field of medical genomics involves translating high throughput genetic methods to the cl...
none3The recent improvement of the high-throughput sequencing technologies is having a strong impact...
New sequencing technology has enabled the identification of thousands of single nucleotide polymorph...
The field of human genetics has been radically changed by the introduction of massive parallel seque...
Despite thousands of genetic loci identified to date, a large proportion of genetic variation predis...
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for...
AbstractThe completion of the human genome sequence in 2003 clearly marked the beginning of a new er...
Incorporating information about common genetic variants may help improve the design and analysis of ...
Genome and exome sequencing in large cohorts enables characterization of the role of rare variation ...
Novel high-throughput sequencing technologies generate largescale genomic data and are used extensiv...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Rapid methodological advances in statistical and computational genomics have enabled researchers to ...
Collectively, rare genetic disorders affect a substantial portion of the world's population. In most...
Advances in DNA sequencing technology have resulted in the ability to generate genetic data at costs...
Genome sequencing is enabling precision medicine-tailoring treatment to the unique constellation of ...
AbstractThe field of medical genomics involves translating high throughput genetic methods to the cl...
none3The recent improvement of the high-throughput sequencing technologies is having a strong impact...
New sequencing technology has enabled the identification of thousands of single nucleotide polymorph...
The field of human genetics has been radically changed by the introduction of massive parallel seque...
Despite thousands of genetic loci identified to date, a large proportion of genetic variation predis...
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for...
AbstractThe completion of the human genome sequence in 2003 clearly marked the beginning of a new er...
Incorporating information about common genetic variants may help improve the design and analysis of ...
Genome and exome sequencing in large cohorts enables characterization of the role of rare variation ...
Novel high-throughput sequencing technologies generate largescale genomic data and are used extensiv...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...