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Abstract Here, we present the updated rSNPBase 3.0 database (http://rsnp3.psych.ac.cn), which provides human SNP-related… Expand Transcription factor binding specificity is crucial for proper target gene regulation. Motif discovery algorithms identify the… Expand MOTIVATION
Genome-wide association studies revealed that most disease-associated single nucleotide polymorphisms (SNPs) are… Expand Single nucleotide polymorphisms (SNPs) represent to the genetics variant most common founded in the human genome. These… Expand We have proposed the RSi Research Cloud (RSi-Cloud), which enables integration of robot services with internet services. Until… Expand Motivation: Determining the functional impact of non-coding disease-associated single nucleotide polymorphisms (SNPs) identified… Expand Motivation: Determining the functional impact of non-coding disease-associated single nucleotide polymorphisms (SNPs) identified… Expand The most common form of genetic variation, single nucleotide polymorphisms or SNPs, can affect the way an individual responds to… Expand We describe a pathogenetic mechanism underlying a variant form of the inherited blood disorder α thalassemia. Association studies… Expand The search for the genetic variations underlying all human phenotypes is in its infancy but must be one of the long term goals of… Expand