We have created the Functional Element SNPs Database (FESD) thatcategorizes functionalelements in human genic regions and provides a set of single nucleotide polymorphisms (SNPs) located within each area. In the FESD, the human genic regions were divided into 10 different functional elements, such as promoter regions, CpG islands, 50-untrans-lated regions (50-UTRs), translation start sites, splice sites, coding exons, introns, translation stop sites, polyadenylation signals and 30-UTRs, and subse-quently, all the known SNPs were assigned to each functional element at their respective position. With theFESDweb interface, userscanselect a setofSNPs in the specific functional elements and get their flank-ingsequences forgenotypingexperiments,w...
Single-nucleotide polymorphisms (SNPs) are the most common form of human genetic variation. The codi...
BACKGROUND: The massive amount of SNP data stored at public internet sites provides unprecedented ac...
X-axis is different DNA functional elements. Y-axis is Log2Counts (Counts mean the number of SNVs). ...
Motivation: Design a new computational tool allowing scientists to functionally annotate newly disco...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
The annotation of the human genome has been a daunting task requiring the creation of innovative met...
Background: Over 4 million single nucleotide polymorphisms (SNPs) are currently rep...
After the sequencing of the human genome is done, enormous genomic information and high-through-put ...
Single nucleotide polymorphisms (SNPs) occur frequently and with a relatively even distribution in t...
The human genome encodes the blueprint of life, but the function of the vast majority of its nearly ...
Deep sequencing has shown that over 90% of human genes undergo alternative splicing. The splicing pr...
Association studies hold great promise for the elucidation of the genetic basis of diseases. Studies...
The single nucleotide polymorphisms (SNPs) in conserved protein regions have been thought to be stro...
With the completion of the human genome sequence, attention turned to identifying and annotating its...
The human genome encodes the blueprint of life, but the function of the vast majority of its nearly ...
Single-nucleotide polymorphisms (SNPs) are the most common form of human genetic variation. The codi...
BACKGROUND: The massive amount of SNP data stored at public internet sites provides unprecedented ac...
X-axis is different DNA functional elements. Y-axis is Log2Counts (Counts mean the number of SNVs). ...
Motivation: Design a new computational tool allowing scientists to functionally annotate newly disco...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
The annotation of the human genome has been a daunting task requiring the creation of innovative met...
Background: Over 4 million single nucleotide polymorphisms (SNPs) are currently rep...
After the sequencing of the human genome is done, enormous genomic information and high-through-put ...
Single nucleotide polymorphisms (SNPs) occur frequently and with a relatively even distribution in t...
The human genome encodes the blueprint of life, but the function of the vast majority of its nearly ...
Deep sequencing has shown that over 90% of human genes undergo alternative splicing. The splicing pr...
Association studies hold great promise for the elucidation of the genetic basis of diseases. Studies...
The single nucleotide polymorphisms (SNPs) in conserved protein regions have been thought to be stro...
With the completion of the human genome sequence, attention turned to identifying and annotating its...
The human genome encodes the blueprint of life, but the function of the vast majority of its nearly ...
Single-nucleotide polymorphisms (SNPs) are the most common form of human genetic variation. The codi...
BACKGROUND: The massive amount of SNP data stored at public internet sites provides unprecedented ac...
X-axis is different DNA functional elements. Y-axis is Log2Counts (Counts mean the number of SNVs). ...