In silico detection of sequence variations modifying transcriptional regulation
about
Advances in translational bioinformatics: computational approaches for the hunting of disease genesCandidate gene association studies: a comprehensive guide to useful in silico toolsBioinformatics for personal genome interpretationHaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variantsCis-regulatory somatic mutations and gene-expression alteration in B-cell lymphomas.Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach.On the identification of potential regulatory variants within genome wide association candidate SNP sets.Human variation in short regions predisposed to deep evolutionary conservation.Genomic features defining exonic variants that modulate splicing.Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sampleRare and common regulatory variation in population-scale sequenced human genomesPost-GWAS functional characterization of susceptibility variants for chronic lymphocytic leukemia.Large-scale computational identification of regulatory SNPs with rSNP-MAPPER.SuRFing the genomics wave: an R package for prioritising SNPs by functionalityChapter 15: disease gene prioritization.A common polymorphism in the promoter region of the TNFSF4 gene is associated with lower allele-specific expression and risk of myocardial infarction.Bioinformatics challenges for personalized medicineIdentifying functional single nucleotide polymorphisms in the human CArGomeIdentification of cis-regulatory sequence variations in individual genome sequences.Obesity-related known and candidate SNP markers can significantly change affinity of TATA-binding protein for human gene promoters.A systematic, large-scale comparison of transcription factor binding site models.Candidate SNP markers of aggressiveness-related complications and comorbidities of genetic diseases are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters.atSNP: transcription factor binding affinity testing for regulatory SNP detection.Clinical implications of human population differences in genome-wide rates of functional genotypesCandidate SNP Markers of Gender-Biased Autoimmune Complications of Monogenic Diseases Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene PromotersHighly individual methylation patterns of alternative glucocorticoid receptor promoters suggest individualized epigenetic regulatory mechanismsLack of correlation between in silico projection of function and quantitative real-time PCR-determined gene expression levels in colon tissue.Candidate SNP Markers of Chronopathologies Are Predicted by a Significant Change in the Affinity of TATA-Binding Protein for Human Gene Promoters.Predicting functional regulatory polymorphisms.A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular diseaseImpact of DNA-binding position variants on yeast gene expression.Evaluating the impact of single nucleotide variants on transcription factor binding.SNP2TFBS - a database of regulatory SNPs affecting predicted transcription factor binding site affinity.A Functional IL22 Polymorphism (rs2227473) Is Associated with Predisposition to Childhood Cerebral Malaria.Prediction of functional regulatory SNPs in monogenic and complex disease.rSNPBase: a database for curated regulatory SNPs.Statistical analysis strategies for association studies involving rare variants.Tumour necrosis factor gene polymorphism and disease prevalence.DNA sequence variation and regulation of genes involved in pathogenesis of pulmonary tuberculosis.Identification of candidate regulatory SNPs by combination of transcription-factor-binding site prediction, SNP genotyping and haploChIP
P2860
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P2860
In silico detection of sequence variations modifying transcriptional regulation
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
In silico detection of sequence variations modifying transcriptional regulation
@ast
In silico detection of sequence variations modifying transcriptional regulation
@en
In silico detection of sequence variations modifying transcriptional regulation
@nl
type
label
In silico detection of sequence variations modifying transcriptional regulation
@ast
In silico detection of sequence variations modifying transcriptional regulation
@en
In silico detection of sequence variations modifying transcriptional regulation
@nl
prefLabel
In silico detection of sequence variations modifying transcriptional regulation
@ast
In silico detection of sequence variations modifying transcriptional regulation
@en
In silico detection of sequence variations modifying transcriptional regulation
@nl
P2093
P2860
P50
P3181
P1476
In silico detection of sequence variations modifying transcriptional regulation
@en
P2093
David Arenillas
Malin C Andersen
Stuart Lithwick
P2860
P3181
P356
10.1371/JOURNAL.PCBI.0040005
P407
P577
2008-01-01T00:00:00Z