PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes
about
The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factorsAfrican signatures of recent positive selection in human FOXI1SNPs associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's diseaseCardioGxE, a catalog of gene-environment interactions for cardiometabolic traitsGWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery diseaseGenome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseCandidate gene association studies: a comprehensive guide to useful in silico toolsComputational and statistical approaches to analyzing variants identified by exome sequencingAssociation of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disordersIn silico analysis of single nucleotide polymorphism (SNPs) in human β-globin geneNext generation tools for the annotation of human SNPsGWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.First- and second-shell metal binding residues in human proteins are disproportionately associated with disease-related SNPs.Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approachSNPLogic: an interactive single nucleotide polymorphism selection, annotation, and prioritization system.Cytokine gene variations associated with subsyndromal depressive symptoms in patients with breast cancerNext station in microarray data analysis: GEPAS.Computational refinement of functional single nucleotide polymorphisms associated with ATM geneiHAP--integrated haplotype analysis pipeline for characterizing the haplotype structure of genesGenome-wide survey of allele-specific splicing in humans.Genetic polymorphisms are associated with serum levels of sex hormone binding globulin in postmenopausal women.Association between polymorphisms in RMI1, TOP3A, and BLM and risk of cancer, a case-control study.Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancerGeneration and analysis of a 29,745 unique Expressed Sequence Tags from the Pacific oyster (Crassostrea gigas) assembled into a publicly accessible database: the GigasDatabase.FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databasesVariations in potassium channel genes are associated with breast pain in women prior to breast cancer surgery.Cytokine gene variations associated with trait and state anxiety in oncology patients and their family caregivers.dPORE-miRNA: polymorphic regulation of microRNA genes.Associations between cytokine genes and a symptom cluster of pain, fatigue, sleep disturbance, and depression in patients prior to breast cancer surgeryCytokine gene associations with self-report ratings of morning and evening fatigue in oncology patients and their family caregivers.Cytokine gene variation is associated with depressive symptom trajectories in oncology patients and family caregivers.A two-phase case-control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22.Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins.ICOS gene polymorphisms are associated with sporadic breast cancer: a case-control studyA polymorphism near IGF1 is associated with body composition and muscle function in women from the Health, Aging, and Body Composition Study.Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencingSingle nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort.Investigating the structural impacts of I64T and P311S mutations in APE1-DNA complex: a molecular dynamics approach.Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT StudyVARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing
P2860
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P2860
PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
PupaSuite: finding functional ...... arge-scale genotyping purposes
@ast
PupaSuite: finding functional ...... arge-scale genotyping purposes
@en
PupaSuite: finding functional ...... arge-scale genotyping purposes
@nl
type
label
PupaSuite: finding functional ...... arge-scale genotyping purposes
@ast
PupaSuite: finding functional ...... arge-scale genotyping purposes
@en
PupaSuite: finding functional ...... arge-scale genotyping purposes
@nl
prefLabel
PupaSuite: finding functional ...... arge-scale genotyping purposes
@ast
PupaSuite: finding functional ...... arge-scale genotyping purposes
@en
PupaSuite: finding functional ...... arge-scale genotyping purposes
@nl
P2093
P2860
P50
P356
P1476
PupaSuite: finding functional ...... arge-scale genotyping purposes
@en
P2093
Frederic Rousseau
Hernán Dopazo
Leonardo Arbiza
Lucía Conde
P2860
P304
P356
10.1093/NAR/GKL071
P407
P433
Web Server issue
P577
2006-07-01T00:00:00Z