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PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level
被引:70
作者:

Conde, L
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Vaquerizas, JM
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Santoyo, J
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Al-Shahrour, F
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Ruiz-Llorente, S
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Robledo, M
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机构: Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain

Dopazo, J
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机构:
Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain
机构:
[1] Ctr Nacl Invest Oncol, Bioinformat Unit, Madrid, Spain
[2] Ctr Nacl Invest Oncol, Hereditary Endocrine Canc Grp, Madrid, Spain
关键词:
D O I:
10.1093/nar/gkh438
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
We have developed a web tool, PupaSNP Finder (PupaSNP for short), for high-throughput searching for single nucleotide polymorphisms (SNPs) with potential phenotypic effect. PupaSNP takes as its input lists of genes (or generates them from chromosomal coordinates) and retrieves SNPs that could affect the conserved regions that the cellular machinery uses for the correct processing of genes (intron/exon boundaries or exonic splicing enhancers), predicted transcription factor binding sites (TFBS) and changes in amino acids in the proteins. The program uses the mapping of SNPs in the genome provided by Ensembl. Additionally, user-defined SNPs (not yet mapped in the genome) can be easily provided to the program. Also, additional functional information from Gene Ontology, OMIM and homologies in other model organisms is provided. In contrast to other programs already available, which focus only on SNPs with possible effect in the protein, PupaSNP includes SNPs with possible transcriptional effect. PupaSNP will be of significant help in studies of multifactorial disorders, where the use of functional SNPs will increase the sensitivity of identification of the genes responsible for the disease. The PupaSNP web interface is accessible through http://pupasnp.bioinfo.cnio.es.
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页码:W242 / W248
页数:7
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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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h-index: 0
机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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h-index: 0
机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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h-index: 0
机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England

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机构: Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England