The human genome contains millions of genetic variants that make each individual unique. Some variants affect eye colour or blood type and others affect hereditary diseases. The DNA sequence may also include a pathogenic sequence variant that causes various disruptions in the function of the gene. The disruptions manifest themselves as hereditary diseases. Blueprint Genetics from Finland classifies genetic variants found in the genome from patient samples and analyses their connection to the described symptoms of the patients
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
Humans differ from each other in their genomes by <1 %. This determines the difference in suscept...
DNA sequencing has revolutionized biological and medical research, and is poised to have a similar i...
DNA testing in patients suspected of having a genetic disorder will not always result in clear findi...
Inherited diseases are health problems caused by one or more abnormalities in the genome. It can be ...
Identifying the causes of similarities and differences in genetic disease prevalence among humans is...
Advances in DNA sequencing technology have resulted in the ability to generate genetic data at costs...
AbstractThe field of medical genomics involves translating high throughput genetic methods to the cl...
The advent of recombinant DNA technology has contributed enormously to our understanding of human ge...
Purpose: To explore two approaches for making the human genome more accessible and useful to practic...
The analysis of human genetic variability can lead to the comprehension of medical issues and to the...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
Natural genetic material may shed light on gene expression mechanisms and aid in the detection of ge...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
Humans differ from each other in their genomes by <1 %. This determines the difference in suscept...
DNA sequencing has revolutionized biological and medical research, and is poised to have a similar i...
DNA testing in patients suspected of having a genetic disorder will not always result in clear findi...
Inherited diseases are health problems caused by one or more abnormalities in the genome. It can be ...
Identifying the causes of similarities and differences in genetic disease prevalence among humans is...
Advances in DNA sequencing technology have resulted in the ability to generate genetic data at costs...
AbstractThe field of medical genomics involves translating high throughput genetic methods to the cl...
The advent of recombinant DNA technology has contributed enormously to our understanding of human ge...
Purpose: To explore two approaches for making the human genome more accessible and useful to practic...
The analysis of human genetic variability can lead to the comprehension of medical issues and to the...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
Natural genetic material may shed light on gene expression mechanisms and aid in the detection of ge...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
Humans differ from each other in their genomes by <1 %. This determines the difference in suscept...
DNA sequencing has revolutionized biological and medical research, and is poised to have a similar i...