With the advent of large-scale next-generation sequencing initiatives, there is an increasing importance to interpret and understand the potential phenotypic influence of identified genetic variation and its significance in the human genome. Bioinformatics analyses can provide useful information to assist with variant interpretation. This review provides an overview of tools/resources currently available, and how they can help predict the impact of genetic variation at the deoxyribonucleic acid, ribonucleic acid, and protein level
In genome medicine, which is now being implemented in medical care, variants detected by genome anal...
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for...
BACKGROUND: With the recent growth of information on sequence variations in the human genome, predic...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
An international consortium released the first draft sequence of the human genome 10 years ago. Alth...
In studies of human genome variation, researchers attempt to identify the DNA sequence differences b...
Precision medicine programs to identify clinically relevant genetic variation have been revolutioniz...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Molecular biology is currently a fast-advancing science. Sequencing techniques are getting cheaper, ...
This thesis is divided into three parts, united under the general theme of bioinformatics tool devel...
[EN]The analysis of genetic data has always been a problem due to the large amount of information av...
AbstractThe study of DNA sequence variation has been transformed by recent advances in DNA sequencin...
Indiana University-Purdue University Indianapolis (IUPUI)The information gained from sequencing of t...
Identification of functional genetic variation associated with increased susceptibility to complex d...
Elucidating the content of a DNA sequence is critical to deeper understand and decode the genetic in...
In genome medicine, which is now being implemented in medical care, variants detected by genome anal...
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for...
BACKGROUND: With the recent growth of information on sequence variations in the human genome, predic...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
An international consortium released the first draft sequence of the human genome 10 years ago. Alth...
In studies of human genome variation, researchers attempt to identify the DNA sequence differences b...
Precision medicine programs to identify clinically relevant genetic variation have been revolutioniz...
All human beings are approximately 99.9% similar in their DNA sequences. The 0.1% contains different...
Molecular biology is currently a fast-advancing science. Sequencing techniques are getting cheaper, ...
This thesis is divided into three parts, united under the general theme of bioinformatics tool devel...
[EN]The analysis of genetic data has always been a problem due to the large amount of information av...
AbstractThe study of DNA sequence variation has been transformed by recent advances in DNA sequencin...
Indiana University-Purdue University Indianapolis (IUPUI)The information gained from sequencing of t...
Identification of functional genetic variation associated with increased susceptibility to complex d...
Elucidating the content of a DNA sequence is critical to deeper understand and decode the genetic in...
In genome medicine, which is now being implemented in medical care, variants detected by genome anal...
Genomic variations and phenotypic diversity are closely linked and form the underlying mechanism for...
BACKGROUND: With the recent growth of information on sequence variations in the human genome, predic...