AbstractOne of the long-standing challenges in biology is to understand how non-synonymous single nucleotide polymorphisms (nsSNPs) change protein structure and further affect their function. While it is impractical to solve all the mutated protein structures experimentally, it is quite feasible to model the mutated structures in silico. Toward this goal, we built a publicly available structure database resource (SNP2Structure, https://apps.icbi.georgetown.edu/snp2structure) focusing on missense mutations, msSNP. Compared with web portals with similar aims, SNP2Structure has the following major advantages. First, our portal offers direct comparison of two related 3D structures. Second, the protein models include all interacting molecules in...
The Single Amino Acid Polymorphism database (SAAPdb) is a new resource for the analysis and visualiz...
The translation of personal genomics to precision medicine depends on the accurate interpretation of...
Background: Genome-wide association studies of common diseases for common, low penetrance causal var...
One of the long-standing challenges in biology is to understand how non-synonymous single nucleotide...
The prediction of the effects of nonsynonymous single nucleotide polymorphisms (nsSNPs) on function ...
The prediction of the effects of nonsynonymous single nucleotide polymorphisms (nsSNPs) on function ...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
Background: The phenotypic effects of sequence variations in protein-coding regions come about prima...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
One of the two objectives of this thesis is to design a new method that predicts the structural effe...
Background: Single Nucleotide Polymorphisms (SNPs) are an important source of human genome variabili...
Single-nucleotide polymorphisms (SNPs) are single-base variants that contribute to human biological ...
Background: Single Nucleotide Polymorphisms (SNPs) are an important source of human genome variabili...
The translation of personal genomics to precision medicine depends on the accurate interpretation of...
The Single Amino Acid Polymorphism database (SAAPdb) is a new resource for the analysis and visualiz...
The translation of personal genomics to precision medicine depends on the accurate interpretation of...
Background: Genome-wide association studies of common diseases for common, low penetrance causal var...
One of the long-standing challenges in biology is to understand how non-synonymous single nucleotide...
The prediction of the effects of nonsynonymous single nucleotide polymorphisms (nsSNPs) on function ...
The prediction of the effects of nonsynonymous single nucleotide polymorphisms (nsSNPs) on function ...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
Background: The phenotypic effects of sequence variations in protein-coding regions come about prima...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human ...
One of the two objectives of this thesis is to design a new method that predicts the structural effe...
Background: Single Nucleotide Polymorphisms (SNPs) are an important source of human genome variabili...
Single-nucleotide polymorphisms (SNPs) are single-base variants that contribute to human biological ...
Background: Single Nucleotide Polymorphisms (SNPs) are an important source of human genome variabili...
The translation of personal genomics to precision medicine depends on the accurate interpretation of...
The Single Amino Acid Polymorphism database (SAAPdb) is a new resource for the analysis and visualiz...
The translation of personal genomics to precision medicine depends on the accurate interpretation of...
Background: Genome-wide association studies of common diseases for common, low penetrance causal var...