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snp reference database  (Celera)

 
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    Celera snp reference database
    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/snp+reference+database/pmc01895132-24-31-30
    Average 90 stars, based on 1 article reviews
    snp reference database - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Selection:

    Article Title: Association of KLK3 (PSA) genetic variants with prostate cancer risk and PSA levels
    Article Snippet: .. SNP selection and genotyping We identified bona fide and suitably informative SNPs from among those represented in independently derived SNP databases prior to the completion of The International HapMap Project, namely the open access NCBI dbSNP ( http://www.ncbi.nlm.nih.gov/projects/SNP/ ) and Japanese SNP ( http://snp.ims.u-tokyo.ac.jp/ ) databases as well as the Celera SNP Reference Database ( 29 ). ..

    Derivative Assay:

    Article Title: Association of KLK3 (PSA) genetic variants with prostate cancer risk and PSA levels
    Article Snippet: .. SNP selection and genotyping We identified bona fide and suitably informative SNPs from among those represented in independently derived SNP databases prior to the completion of The International HapMap Project, namely the open access NCBI dbSNP ( http://www.ncbi.nlm.nih.gov/projects/SNP/ ) and Japanese SNP ( http://snp.ims.u-tokyo.ac.jp/ ) databases as well as the Celera SNP Reference Database ( 29 ). ..

    Article Title: Association of KLK3 (PSA) genetic variants with prostate cancer risk and PSA levels
    Article Snippet: .. We identified bona fide and suitably informative SNPs from among those represented in independently derived SNP databases prior to the completion of The International HapMap Project, namely the open access NCBI dbSNP ( http://www.ncbi.nlm.nih.gov/projects/SNP/ ) and Japanese SNP ( http://snp.ims.u-tokyo.ac.jp/ ) databases as well as the Celera SNP Reference Database ( 29 ). ..

    Software:

    Article Title: Bio-Almanac
    Article Snippet: Juno Online Services Inc. today announced that it has signed a letter of intent with LaunchCyte LLC, a pioneering bioinformatics incubator, setting forth terms for use of the Juno Virtual Supercomputer by LaunchCyte and its portfolio companies.. Juno is one of the nation’s largest Internet access providers, with 15.9 million total registered subscribers as of March 31, 2001, and 4.1 million active subscribers in the month of March.. The Juno Virtual Supercomputer Project is a distributed computing effort designed to harness unused processing power associated with the computers of Juno’s subscriber base in order to execute computationally intensive biomedical and other applications on behalf of commercial clients and research institutions.



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    reference snp data  (Biotechnology Information)
    86
    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, 2026-10
    86/100 stars
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    human snp reference data database  (Celera)
    90
    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, 2026-10
    90/100 stars
    		  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