The analysis of human genetic variability can lead to the comprehension of medical issues and to the development of personalized therapeutic protocols. Single nucleotide polymorphisms, are the most common type of human genetic variation and have been associated to disease development and phenotype forecasting. The recent technologies for DNA sequencing and bioinformatic analysis are now giving the opportunity to develop new diagnostic and prevention approaches also through health promotion protocols. The genetic data management is at the same time underlining technical limitations and old ethical issues
Pharmacogenomics is the study of how genetic makeup determines the response to a therapeutic interve...
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
The human genome contains millions of genetic variants that make each individual unique. Some varian...
The genomic revolution has generated an extraordinary resource, the catalog of variation within the ...
AbstractGenome-wide patterns of variation across individuals provide most powerful source of data fo...
After the sequencing of the human genome is done, enormous genomic information and high-through-put ...
In this review, we consider the motivation behind contemporary single nucleotide polymorphism (SNP) ...
Single nucleotide polymorphisms (SNP) represent the largest source of diversity in the human genome....
Single nucleotide polymorphisms (SNPs) are places along the chromosomes where the genetic code tends...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
AbstractThe completion of the human genome sequence in 2003 clearly marked the beginning of a new er...
Advances in high-throughput sequencing, genotyping, and characterization of haplotype diversity are ...
In studies of human genome variation, researchers attempt to identify the DNA sequence differences b...
The application of sequencing technologies has steadily increased over the past few years. This has ...
Single nucleotide polymorphisms (SNPs) have been classically used for dissecting various human compl...
Pharmacogenomics is the study of how genetic makeup determines the response to a therapeutic interve...
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
The human genome contains millions of genetic variants that make each individual unique. Some varian...
The genomic revolution has generated an extraordinary resource, the catalog of variation within the ...
AbstractGenome-wide patterns of variation across individuals provide most powerful source of data fo...
After the sequencing of the human genome is done, enormous genomic information and high-through-put ...
In this review, we consider the motivation behind contemporary single nucleotide polymorphism (SNP) ...
Single nucleotide polymorphisms (SNP) represent the largest source of diversity in the human genome....
Single nucleotide polymorphisms (SNPs) are places along the chromosomes where the genetic code tends...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
AbstractThe completion of the human genome sequence in 2003 clearly marked the beginning of a new er...
Advances in high-throughput sequencing, genotyping, and characterization of haplotype diversity are ...
In studies of human genome variation, researchers attempt to identify the DNA sequence differences b...
The application of sequencing technologies has steadily increased over the past few years. This has ...
Single nucleotide polymorphisms (SNPs) have been classically used for dissecting various human compl...
Pharmacogenomics is the study of how genetic makeup determines the response to a therapeutic interve...
Human genetics has progressed at an unprecedented pace during the past 10 years. DNA microarrays cur...
The human genome contains millions of genetic variants that make each individual unique. Some varian...