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Celera celera’s human snp reference database
Celera’s Human Snp Reference Database, supplied by Celera, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+snp+reference+database/celera+snps/pmc01634802-35-19-18
Average 90 stars, based on 1 article reviews
celera’s human snp reference database - by Bioz Stars, 2026-09
90/100 stars

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In Silico:

Article Title: ESR1 and EGF genetic variation in relation to breast cancer risk and survival
Article Snippet: We selected SNPs in the ESR1 and EGF genes and their 20 kb flanking sequences from dbSNP (build 124, [ ]) and Celera databases, aiming for an initial marker density of at least one SNP per 5 kb.

Article Title: Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases
Article Snippet: In this new version of PupaSuite, the database has been updated to analyze the complete set of SNPs cataloged in version 44 of Ensembl , which includes dbSNP ( ) 126 genotype data and Sanger-caller Celera SNPs.

Article Title: Methods for placing, accepting, and filling orders for products and services
Article Snippet: Gene Symbol LocusLink Gene Name RefSeq Accession AB Assay ID Celera SNP (hCV) Celera gene (hCG) Celera transcript (hCT) Celera protein (hCP) Chromosome Cytoband LocusLink ID In addition, it is possible to filter the search by the specific SNP type which include: acceptor splice site coding region donor splice site intergenic/unknown intron mis-sense mutation nonsense mutation putative utr (untranslated region) 3 putative utr 5 repeats silent mutation utr 3 utr 5 In addition, it is possible to search all these SNP types together.

Article Title: Roles of the ubiquitin peptidase USP18 in multiple sclerosis and the response to interferon-β treatment.
Article Snippet: the response to interferon-b treatment S. Malhotra, C. Morcillo-Su arez, R. Nurtdinov, J. Rio, E. Sarro, M. Moreno, J. Castill o, A. Navarro, X. Montalban and M. Comabella Servei de Neurologia/Neuroimmunologia, Centre d’Esclerosi M ultiple de Catalunya (CEM-Cat), Hospital Universitari Vall d′Hebron (HUVH), Barcelona; Institute of Evolutionary Biology (UPF-CSIC), Barcelona; National Institute for Bioinformatics, Universitat Pompeu Fabra, Barcelona; Fisiopatolog ıa Renal, VHIR – CIBBIM, Nanomedicina, Barcelona; and Instituci o Catalana de Recerca i Estudis Avancats (ICREA), Barcelona, Spain

Article Title: Genome assembly comparison identifies structural variants in the human genome
Article Snippet: First, we found 1,521,291 of 1,591,291 (95.6%) single-nucleotide mismatches to be present in dbSNP; 840,802 of these were Celera-based SNPs, whereas the others were from different projects.

Binding Assay:

Article Title: ESR1 and EGF genetic variation in relation to breast cancer risk and survival
Article Snippet: We selected SNPs in the ESR1 and EGF genes and their 20 kb flanking sequences from dbSNP (build 124, [ ]) and Celera databases, aiming for an initial marker density of at least one SNP per 5 kb.

Article Title: Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases
Article Snippet: In this new version of PupaSuite, the database has been updated to analyze the complete set of SNPs cataloged in version 44 of Ensembl , which includes dbSNP ( ) 126 genotype data and Sanger-caller Celera SNPs.

Article Title: Methods for placing, accepting, and filling orders for products and services
Article Snippet: Gene Symbol LocusLink Gene Name RefSeq Accession AB Assay ID Celera SNP (hCV) Celera gene (hCG) Celera transcript (hCT) Celera protein (hCP) Chromosome Cytoband LocusLink ID In addition, it is possible to filter the search by the specific SNP type which include: acceptor splice site coding region donor splice site intergenic/unknown intron mis-sense mutation nonsense mutation putative utr (untranslated region) 3 putative utr 5 repeats silent mutation utr 3 utr 5 In addition, it is possible to search all these SNP types together.

Article Title: Roles of the ubiquitin peptidase USP18 in multiple sclerosis and the response to interferon-β treatment.
Article Snippet: the response to interferon-b treatment S. Malhotra, C. Morcillo-Su arez, R. Nurtdinov, J. Rio, E. Sarro, M. Moreno, J. Castill o, A. Navarro, X. Montalban and M. Comabella Servei de Neurologia/Neuroimmunologia, Centre d’Esclerosi M ultiple de Catalunya (CEM-Cat), Hospital Universitari Vall d′Hebron (HUVH), Barcelona; Institute of Evolutionary Biology (UPF-CSIC), Barcelona; National Institute for Bioinformatics, Universitat Pompeu Fabra, Barcelona; Fisiopatolog ıa Renal, VHIR – CIBBIM, Nanomedicina, Barcelona; and Instituci o Catalana de Recerca i Estudis Avancats (ICREA), Barcelona, Spain

Article Title: Genome assembly comparison identifies structural variants in the human genome
Article Snippet: First, we found 1,521,291 of 1,591,291 (95.6%) single-nucleotide mismatches to be present in dbSNP; 840,802 of these were Celera-based SNPs, whereas the others were from different projects.

Functional Assay:

Article Title: ESR1 and EGF genetic variation in relation to breast cancer risk and survival
Article Snippet: We selected SNPs in the ESR1 and EGF genes and their 20 kb flanking sequences from dbSNP (build 124, [ ]) and Celera databases, aiming for an initial marker density of at least one SNP per 5 kb.

Article Title: Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases
Article Snippet: In this new version of PupaSuite, the database has been updated to analyze the complete set of SNPs cataloged in version 44 of Ensembl , which includes dbSNP ( ) 126 genotype data and Sanger-caller Celera SNPs.

Article Title: Methods for placing, accepting, and filling orders for products and services
Article Snippet: Gene Symbol LocusLink Gene Name RefSeq Accession AB Assay ID Celera SNP (hCV) Celera gene (hCG) Celera transcript (hCT) Celera protein (hCP) Chromosome Cytoband LocusLink ID In addition, it is possible to filter the search by the specific SNP type which include: acceptor splice site coding region donor splice site intergenic/unknown intron mis-sense mutation nonsense mutation putative utr (untranslated region) 3 putative utr 5 repeats silent mutation utr 3 utr 5 In addition, it is possible to search all these SNP types together.

Article Title: Roles of the ubiquitin peptidase USP18 in multiple sclerosis and the response to interferon-β treatment.
Article Snippet: the response to interferon-b treatment S. Malhotra, C. Morcillo-Su arez, R. Nurtdinov, J. Rio, E. Sarro, M. Moreno, J. Castill o, A. Navarro, X. Montalban and M. Comabella Servei de Neurologia/Neuroimmunologia, Centre d’Esclerosi M ultiple de Catalunya (CEM-Cat), Hospital Universitari Vall d′Hebron (HUVH), Barcelona; Institute of Evolutionary Biology (UPF-CSIC), Barcelona; National Institute for Bioinformatics, Universitat Pompeu Fabra, Barcelona; Fisiopatolog ıa Renal, VHIR – CIBBIM, Nanomedicina, Barcelona; and Instituci o Catalana de Recerca i Estudis Avancats (ICREA), Barcelona, Spain

Article Title: Genome assembly comparison identifies structural variants in the human genome
Article Snippet: First, we found 1,521,291 of 1,591,291 (95.6%) single-nucleotide mismatches to be present in dbSNP; 840,802 of these were Celera-based SNPs, whereas the others were from different projects.



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