FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization. - Wikidata - thesis-toulmin - TriplyDB

FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.

FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.

http://www.wikidata.org/entity/Q34548039

about

Common genetic variation and the control of HIV-1 in humans Polymorphisms in the estrogen receptor 1 and vitamin C and matrix metalloproteinase gene families are associated with susceptibility to lymphoma Genetic associations with sporadic neuroendocrine tumor risk A Large-scale genetic association study of esophageal adenocarcinoma risk Advances in translational bioinformatics: computational approaches for the hunting of disease genes High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men Application of CRISPR/Cas9 Technology to HBV A review of post-GWAS prioritization approaches Host Genetics, Steatosis and Insulin Resistance among African Americans and Caucasian Americans with Hepatitis C Virus Genotype-1 Infection Cooperation of DLC1 and CDK6 affects breast cancer clinical outcome Circadian genes and breast cancer susceptibility in rotating shift workers Next generation tools for the annotation of human SNPs A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303 Genome-wide association study implicates PARD3B-based AIDS restriction A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility Identification of functional SNPs in BARD1 gene and in silico analysis of damaging SNPs: based on data procured from dbSNP database Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.Evolution- and structure-based computational strategy reveals the impact of deleterious missense mutations on MODY 2 (maturity-onset diabetes of the young, type 2)Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies Prediction of functionally significant single nucleotide polymorphisms [SNPs] in PTEN tumor suppressor gene: An in silico approach.Meet me halfway: when genomics meets structural bioinformatics.Path to facilitate the prediction of functional amino acid substitutions in red blood cell disorders--a computational approach CUBN is a gene locus for albuminuria.Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15 Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.Single nucleotide polymorphisms in the CD40 gene associate with the disease susceptibility and severity in knee osteoarthritis in the Chinese Han population: a case-control study.Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population.Computational refinement of functional single nucleotide polymorphisms associated with ATM gene Detection of the inferred interaction network in hepatocellular carcinoma from EHCO (Encyclopedia of Hepatocellular Carcinoma genes Online).Association between CFL1 gene polymorphisms and spina bifida risk in a California population.Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study.Association analysis of WNT10B with bone mass and structure among individuals of African ancestry Functional analysis of novel SNPs and mutations in human and mouse genomes.Genetic polymorphisms are associated with serum levels of sex hormone binding globulin in postmenopausal women.Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche.Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.Toll-like receptor 2 gene polymorphisms, pulmonary tuberculosis, and natural killer cell counts.

P2860

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FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.

http://www.wikidata.org/entity/Q34548039

description

2006 nî lūn-bûn

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2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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FASTSNP: an always up-to-date ...... n analysis and prioritization.

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Nucleic Acids Research

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Adam Yao

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Chia-Hung Liu

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Chuan-Kun Liu

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Chun-Nan Hsu

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Hui-Hung Wang

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Jen-Jie Chiou

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Wen-Hsien Tseng

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Yi-Jung Lin

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P2860

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals

Target SNP selection in complex disease association studies

The HUGO Gene Nomenclature Database, 2006 updates.

The International HapMap Project

The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003

The UCSC Genome Browser Database

Characterization of single-nucleotide polymorphisms in coding regions of human genes

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

RESCUE-ESE identifies candidate exonic splicing enhancers in vertebrate exons

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10.1093/NAR/GKL236

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Web Server issue

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34

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Yuan-Tsong Chen

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2006-07-01T00:00:00Z

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6940907

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