國家衛生研究院 NHRI:Item 3990099045/11456
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 912472      Online Users : 1202
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version


    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/11456


    Title: Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
    Authors: Natarajan, P;Peloso, GM;Zekavat, SM;Montasser, M;Ganna, A;Chaffin, M;Khera, AV;Zhou, W;Bloom, JM;Engreitz, JM;Ernst, J;O’Connell, JR;Ruotsalainen, SE;Alver, M;Manichaikul, A;Johnson, WC;Perry, JA;Poterba, T;Seed, C;Surakka, IL;Esko, T;Ripatti, S;Salomaa, V;Correa, A;Vasan, RS;Kellis, M;Neale, BM;Lander, ES;Abecasis, G;Mitchell, B;Rich, SS;Wilson, JG;Cupples, LA;Rotter, JI;Willer, CJ;Kathiresan, S;Abe, N;Albert, C;Allred, NNP;Almasy, L;Alonso, A;Ament, S;Anderson, P;Anugu, P;Applebaum-Bowden, D;Arking, D;Arnett, DK;Ashley-Koch, A;Aslibekyan, S;Assimes, T;Auer, P;Avramopoulos, D;Barnard, J;Barnes, K;Barr, RG;Barron-Casella, E;Beaty, T;Becker, D;Becker, L;Beer, R;Begum, F;Beitelshees, A;Benjamin, E;Bezerra, M;Bielak, L;Bis, J;Blackwell, T;Blangero, J;Boerwinkle, E;Borecki, I;Bowler, R;Brody, J;Broeckel, U;Broome, J;Bunting, K;Burchard, E;Cardwell, J;Carty, C;Casaburi, R;Casella, J;Chang, C;Chasman, D;Chavan, S;Chen, BJ;Chen, WM;Chen, YDI;Cho, M;Choi, SH;Chuang, LM;Chung, M;Cornell, E;Crandall, C;Crapo, J;Curran, J;Curtis, J;Custer, B;Damcott, C;Darbar, D;Das, S;David, S, .;et al.
    Contributors: Institute of Population Health Sciences
    Abstract: Large-scale deep-coverage whole-genome sequencing (WGS) is now feasible and offers potential advantages for locus discovery. We perform WGS in 16,324 participants from four ancestries at mean depth >29X and analyze genotypes with four quantitative traits—plasma total cholesterol, low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol, and triglycerides. Common variant association yields known loci except for few variants previously poorly imputed. Rare coding variant association yields known Mendelian dyslipidemia genes but rare non-coding variant association detects no signals. A high 2M-SNP LDL-C polygenic score (top 5th percentile) confers similar effect size to a monogenic mutation (~30 mg/dl higher for each); however, among those with severe hypercholesterolemia, 23% have a high polygenic score and only 2% carry a monogenic mutation. At these sample sizes and for these phenotypes, the incremental value of WGS for discovery is limited but WGS permits simultaneous assessment of monogenic and polygenic models to severe hypercholesterolemia.
    Date: 2018-08-23
    Relation: Nature Communications. 2018 Aug 23;9:Article number 3391.
    Link to: http://dx.doi.org/10.1038/s41467-018-05747-8
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=2041-1723&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000442521500016
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85052245414
    Appears in Collections:[Chao A. Hsiung] Periodical Articles

    Files in This Item:

    File Description SizeFormat
    SCP85052245414.pdf914KbAdobe PDF242View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback