SummaryThe Probabilistic Identification of Causal SNPs (PICS) algorithm and web application was developed as a fine-mapping tool to determine the likelihood that each single nucleotide polymorphism (SNP) in LD with a reported index SNP is a true causal polymorphism. PICS is notable for its ability to identify candidate causal SNPs within a locus using only the index SNP, which are widely available from published GWAS, whereas other methods require full summary statistics or full genotype data. However, the original PICS web application operates on a single SNP at a time, with slow performance, severely limiting its usability. We have developed a next-generation PICS tool, PICS2, which enables performance of PICS analyses of large batches of...
The recent advances in genomic technologies, have made it possible to collect large-scale informatio...
Genome-wide association studies (GWAS) use custom SNP arrays that provide ef- fective genetic covera...
Motivation: With the knowledge of large number of SNPs in human genome and the fast development in h...
Abstract Background Linkage disequilibrium (LD) mapping is commonly used to evaluate markers for gen...
Summary: We present MutaGeneSys: a system that uses genomewide genotype data for disease prediction....
Genome-wide association studies have been performed extensively in the last few years, resulting in ...
Background: Recent advances in sequencing technologies promise to provide a better understanding of ...
Background: Understanding the mapping precision of genome-wide association studies (GWAS), that is t...
ABSTRACT: Genome-wide association studies allow detection of non-genotyped disease-causing variants ...
Genome-wide association study (GWAS) is widely utilized to identify genes involved in human complex ...
Remarkable advances have occurred recently in our ability to detect genetic polymorphisms contributi...
Results from genome-wide association studies (GWAS) can be used to infer causal relationships betwee...
AbstractHigh-throughput genotyping chips have produced huge datasets for genome-wide association stu...
Background: Genome-wide association studies (GWAS) based on single nucleotide polymorphisms (SNPs) r...
Summary: We created a fast, robust and general C++ implementation of a single-nucleotide polymorphis...
The recent advances in genomic technologies, have made it possible to collect large-scale informatio...
Genome-wide association studies (GWAS) use custom SNP arrays that provide ef- fective genetic covera...
Motivation: With the knowledge of large number of SNPs in human genome and the fast development in h...
Abstract Background Linkage disequilibrium (LD) mapping is commonly used to evaluate markers for gen...
Summary: We present MutaGeneSys: a system that uses genomewide genotype data for disease prediction....
Genome-wide association studies have been performed extensively in the last few years, resulting in ...
Background: Recent advances in sequencing technologies promise to provide a better understanding of ...
Background: Understanding the mapping precision of genome-wide association studies (GWAS), that is t...
ABSTRACT: Genome-wide association studies allow detection of non-genotyped disease-causing variants ...
Genome-wide association study (GWAS) is widely utilized to identify genes involved in human complex ...
Remarkable advances have occurred recently in our ability to detect genetic polymorphisms contributi...
Results from genome-wide association studies (GWAS) can be used to infer causal relationships betwee...
AbstractHigh-throughput genotyping chips have produced huge datasets for genome-wide association stu...
Background: Genome-wide association studies (GWAS) based on single nucleotide polymorphisms (SNPs) r...
Summary: We created a fast, robust and general C++ implementation of a single-nucleotide polymorphis...
The recent advances in genomic technologies, have made it possible to collect large-scale informatio...
Genome-wide association studies (GWAS) use custom SNP arrays that provide ef- fective genetic covera...
Motivation: With the knowledge of large number of SNPs in human genome and the fast development in h...