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mouse single nucleotide polymorphism (snp) reference database  (Celera)

 
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    Celera mouse single nucleotide polymorphism (snp) reference database
    Mouse Single Nucleotide Polymorphism (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/reference+snp+data/mouse+refsnp+database/pm16179420-112-12-11
    Average 90 stars, based on 1 article reviews
    mouse single nucleotide polymorphism (snp) reference database - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Sequencing:

    Article Title: Mutations in the macrophage scavenger receptor 1 gene alter risk of prostate cancer, asthma, and cardiovascular disease
    Article Snippet: .. Although over 130 and 100 SNPs are listed in NCBI's dbSNP database and Celera's Human RefSNP database, respectively, for the MSR1 gene, none of these reported sequence changes lie in the coding region. ..

    Article Title: Identification of diabetes susceptibility loci in db mice by combined quantitative trait loci analysis and haplotype mapping.
    Article Snippet: .. To define the QTL on Chr 16, we first searched the Celera RefSNP database for interstrain sequence variations between B6 and DBA strains. .. We adopted this approach because the genetic background of the C3H strain is similar to that of the DBA strain in this region on Chr 16 (see Genomics Institute of the Novartis Research Foundation [GNF] SNPview, (http://snp.gnf. org/) (Fig. 4D) [23].

    Article Title: Enhanced cadmium-induced testicular necrosis and renal proximal tubule damage caused by gene-dose increase in a Slc39a8-transgenic mouse line.
    Article Snippet: Bin Wang, Scott N. Schneider, Nadine Dragin, Kuppuswami Girijashanker, Timothy P. Dalton, Lei He, Marian L. Miller, Keith F. Stringer, Manoocher Soleimani, Douglas D. Richardson, and Daniel W. Nebert Department of Environmental Health, and the Center for Environmental Genetics (CEG), University Cincinnati Medical Center, Department of Pathology, Cincinnati Children’s Hospital Medical Center, Department of Internal Medicine, Division of Nephrology and Hypertension, University Cincinnati Medical Center, and Department of Chemistry, University Cincinnati School of Arts and Sciences, Cincinnati Ohio

    other:

    Article Title: Bleomycin-induced pulmonary fibrosis susceptibility genes in AcB/BcA recombinant congenic mice.
    Article Snippet: Lemay, Anne-Marie, and Christina K. Haston.. Bleomycininduced pulmonary fibrosis susceptibility genes in AcB/BcA recombinant congenic mice.. Physiol Genomics 23: 54–61, 2005; 10.1152/physiolgenomics.00095.2005.—The genetic basis of susceptibility to pulmonary fibrosis is largely unknown.

    Construct:

    Article Title: Cis -regulatory variations: A study of SNPs around genes showing cis -linkage in segregating mouse populations
    Article Snippet: .. Since the C3H strain has not yet been sequenced, a complete set of SNPs between the B6 and C3H parental strains used to construct the BXH cross was not available from public sources or the Celera mouse SNP database [ ]. .. Since the C3H strain has not yet been sequenced, a complete set of SNPs between the B6 and C3H parental strains used to construct the BXH cross was not available from public sources or the Celera mouse SNP database [ ].

    Article Title: Identification of diabetes susceptibility loci in db mice by combined quantitative trait loci analysis and haplotype mapping.
    Article Snippet: All SNP sequences within the target region were downloaded from the Celera Mouse GenomeAssembly under the Celera Discovery System (http://www.celera.com). .. The Celera Mouse RefSNP database (release 1.0) was constructed by using data collected at Celera from strains 129x1/SvJ, 129S1/SvImJ, D2J, and B6 mice strains containing 2,566,706 SNPs. ..

    Expressing:

    Article Title: Computer systems and methods for associating genes with traits using cross species data
    Article Snippet: .. It is observed that expression levels for MC3R are not linked to the chromosome 2 locus illustrated in FIG. 20, and there are no SNPS annotated in the exons or introns of the gene between the C57/BL6 and DBA/2J strains in the most recent build of the Celera RefSNP database. ..



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    reference snp data  (Biotechnology Information)
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    Biotechnology Information reference snp data
    A Study design and participant selection. Information of the Arao cohort included MMSE score, diagnostic status, genome-wide <t>SNP</t> <t>data,</t> and APOE genotype. Of 1,526 baseline participants, 1,521 with consent for genetic analysis were selected and subjected to principal component analysis (PCA). After quality control, 1,310 participants were retained for PRS construction. Participants with complete data were included in subsequent analyses ( N = 1,301). B Scatter plot of the first and second principal components (PCs) for study participants ( N = 1,521) and the 1000 Genomes project samples ( N = 2,504). Each point represents an individual based on genome-wide SNP data and is colored by population: AFR, African; AMR, Admixed American; EAS, East Asian; SAS, South Asian; EUR, European.
    Reference Snp Data, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/reference+snp+data/reference+report+snp/med_rxiv__64898__2026__03__26__26349120-62-8-23
    Average 86 stars, based on 1 article reviews
    reference snp data - by Bioz Stars, 2026-11
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    human snp reference data database  (Celera)
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    Celera human snp reference data database
    A Study design and participant selection. Information of the Arao cohort included MMSE score, diagnostic status, genome-wide <t>SNP</t> <t>data,</t> and APOE genotype. Of 1,526 baseline participants, 1,521 with consent for genetic analysis were selected and subjected to principal component analysis (PCA). After quality control, 1,310 participants were retained for PRS construction. Participants with complete data were included in subsequent analyses ( N = 1,301). B Scatter plot of the first and second principal components (PCs) for study participants ( N = 1,521) and the 1000 Genomes project samples ( N = 2,504). Each point represents an individual based on genome-wide SNP data and is colored by population: AFR, African; AMR, Admixed American; EAS, East Asian; SAS, South Asian; EUR, European.
    Human Snp Reference Data 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/reference+snp+data/human+snp+database/us09464320-564-26-25
    Average 90 stars, based on 1 article reviews
    human snp reference data database - by Bioz Stars, 2026-11
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    		  Buy from Supplier

    Image Search Results


    A Study design and participant selection. Information of the Arao cohort included MMSE score, diagnostic status, genome-wide SNP data, and APOE genotype. Of 1,526 baseline participants, 1,521 with consent for genetic analysis were selected and subjected to principal component analysis (PCA). After quality control, 1,310 participants were retained for PRS construction. Participants with complete data were included in subsequent analyses ( N = 1,301). B Scatter plot of the first and second principal components (PCs) for study participants ( N = 1,521) and the 1000 Genomes project samples ( N = 2,504). Each point represents an individual based on genome-wide SNP data and is colored by population: AFR, African; AMR, Admixed American; EAS, East Asian; SAS, South Asian; EUR, European.

    Journal: medRxiv

    Article Title: Population-specific polygenic risk for Alzheimer’s disease is associated with Mini-Mental State Examination-based cognitive decline in a Japanese cohort

    doi: 10.64898/2026.03.26.26349120

    Figure Lengend Snippet: A Study design and participant selection. Information of the Arao cohort included MMSE score, diagnostic status, genome-wide SNP data, and APOE genotype. Of 1,526 baseline participants, 1,521 with consent for genetic analysis were selected and subjected to principal component analysis (PCA). After quality control, 1,310 participants were retained for PRS construction. Participants with complete data were included in subsequent analyses ( N = 1,301). B Scatter plot of the first and second principal components (PCs) for study participants ( N = 1,521) and the 1000 Genomes project samples ( N = 2,504). Each point represents an individual based on genome-wide SNP data and is colored by population: AFR, African; AMR, Admixed American; EAS, East Asian; SAS, South Asian; EUR, European.

    Article Snippet: Curation of SNP data was conducted using a reference SNP data (GCF_000001405.25.vcf.gz) in Variant Call Format (VCF) downloaded from the National Center for Biotechnology Information (NCBI) dbSNP FTP site ( https://ftp.ncbi.nih.gov/snp/latest_release/VCF/ ) ( , ) and dbSNP 147 summarized data from ANNOVAR ( ).

    Techniques: Selection, Diagnostic Assay, Genome Wide, Control