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DNA Resequencing

Known as: Resequencing 
A specific application of gene sequencing that precisely determines the sequence of bases in DNA. Resequencing is used to identify single nucleotide… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Fixed differences in the 3′UTR of buffalo PRNP gene provide binding sites for miRNAs post-transcriptional regulation
Bovine spongiform encephalopathy, a member of transmissible spongiform encephalopathies, has not been reported in buffaloes… 
2015
2015
Correcting Illumina sequencing errors for human data
Summary: We present a new tool to correct sequencing errors in Illumina data produced from high-coverage whole-genome shotgun… 
2012
2012
TREM2 and Alzheimer's disease
although much effort has been made in sequencing autism exomes, it has been difficult to robustly establish asD (autism spectrum… 
2011
2011
Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well…
Gonadotropin-releasing hormone receptor (GNRHR) is a member of the G protein-coupled Ca(2+)-dependent family of receptors. It… 
Review
2011
Review
2011
META-ANALYSIS OF A RARE-VARIANT ASSOCIATION TEST.
Genome-wide assocation studies have often been carried out by meta-analysis rather than by pooling individual-level data. For one… 
2010
2010
Common Susceptibility Variants Examined for Association with Dilated Cardiomyopathy
Rare mutations in more than 20 genes have been suggested to cause dilated cardiomyopathy (DCM), but explain only a small… 
2010
2010
Resequencing of pooled DNA for detecting disease associations with rare variants
A combination of common and rare variants is thought to contribute to genetic susceptibility to complex diseases. Recently, next… 
Highly Cited
2007
Highly Cited
2007
Genetic diversity and function in the human cytosolic sulfotransferases
Amino-acid substitutions, which result from common nonsynonymous (NS) polymorphisms, may dramatically alter the function of the… 
2006
2006
Resequencing of the characterised CTGF gene to identify novel or known variants, and analysis of their association with diabetic nephropathy
AbstractConnective tissue growth factor (CTGF) has been implicated in the pathogenesis of diabetic nephropathy; however, to date… 
2005
2005
CDX2 polymorphisms, RNA expression, and risk of colorectal cancer.
In adult mammals, CDX2 acts as a transcription factor and is expressed in intestinal epithelial cells. Down-regulation of CDX2 is… 
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