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Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.

Elisabeth M van Leeuwen | Aniko Sabo | Joshua C Bis | Jennifer E Huffman | Ani Manichaikul | Albert V Smith | Mary F Feitosa | Serkalem Demissie | Peter K Joshi | Qing Duan | Jonathan Marten | Jan B van Klinken | Ida Surakka | Ilja M Nolte | Weihua Zhang | Hamdi Mbarek | Ruifang Li-Gao | Stella Trompet | Niek Verweij | Evangelos Evangelou | Leo-Pekka Lyytikäinen | Bamidele O Tayo | Joris Deelen | Peter J van der Most | Sander W van der Laan | Dan E Arking | Alanna Morrison | Abbas Dehghan | Oscar H Franco | Albert Hofman | Fernando Rivadeneira | Eric J Sijbrands | Andre G Uitterlinden | Josyf C Mychaleckyj | Archie Campbell | Lynne J Hocking | Sandosh Padmanabhan | Jennifer A Brody | Kenneth M Rice | Charles C White | Tamara Harris | Aaron Isaacs | Harry Campbell | Leslie A Lange | Igor Rudan | Ivana Kolcic | Pau Navarro | Tatijana Zemunik | Veikko Salomaa | LifeLines Cohort Study | Angad S Kooner | Jaspal S Kooner | Benjamin Lehne | William R Scott | Sian-Tsung Tan | Eco J de Geus | Yuri Milaneschi | Brenda W J H Penninx | Gonneke Willemsen | Renée de Mutsert | Ian Ford | Ron T Gansevoort | Marcelo P Segura-Lepe | Olli T Raitakari | Jorma S Viikari | Kjell Nikus | Terrence Forrester | Colin A McKenzie | Anton J M de Craen | Hester M de Ruijter | CHARGE Lipids Working Group | Gerard Pasterkamp | Harold Snieder | Albertine J Oldehinkel | P Eline Slagboom | Richard S Cooper | Mika Kähönen | Terho Lehtimäki | Paul Elliott | Pim van der Harst | J Wouter Jukema | Dennis O Mook-Kanamori | Dorret I Boomsma | John C Chambers | Morris Swertz | Samuli Ripatti | Ko Willems van Dijk | Veronique Vitart | Ozren Polasek | Caroline Hayward | James G Wilson | James F Wilson | Vilmundur Gudnason | Stephen S Rich | Bruce M Psaty | Ingrid B Borecki | Eric Boerwinkle | Jerome I Rotter | L Adrienne Cupples | Cornelia M van Duijn
Journal of medical genetics | 2016

So far, more than 170 loci have been associated with circulating lipid levels through genome-wide association studies (GWAS). These associations are largely driven by common variants, their function is often not known, and many are likely to be markers for the causal variants. In this study we aimed to identify more new rare and low-frequency functional variants associated with circulating lipid levels.

Pubmed ID: 27036123 RIS Download

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100012C
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100010C
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL059367
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100011I
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL087652
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201200036C
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95159
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K002414/1
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85081
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL103612
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100009I
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95160
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL120393
  • Agency: NCRR NIH HHS, United States
    Id: UL1 RR025005
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL080295
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95163
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100008C
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR001079
  • Agency: British Heart Foundation, United Kingdom
    Id: SP/04/002
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100005G
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100008I
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100007C
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268200800007C
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95169
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100011C
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL086694
  • Agency: NHGRI NIH HHS, United States
    Id: U01 HG004402
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L01341X/1
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95164
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR000124
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC55222
  • Agency: Medical Research Council, United Kingdom
    Id: G0700931
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95162
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85086
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL105756
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95168
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK063491
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100006C
  • Agency: Chief Scientist Office, United Kingdom
    Id: CZD/16/6/4
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100005I
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95165
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95161
  • Agency: Medical Research Council, United Kingdom
    Id: MC_PC_U127561128
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL088215
  • Agency: Medical Research Council, United Kingdom
    Id: G0601966
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85082
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95167
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100009C
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85083
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100005C
  • Agency: NHLBI NIH HHS, United States
    Id: HHSN268201100007I
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR000040
  • Agency: Wellcome Trust, United Kingdom
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85079
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC95166
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL117078
  • Agency: NIA NIH HHS, United States
    Id: R01 AG023629
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL087641
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL087700
  • Agency: NHLBI NIH HHS, United States
    Id: N01HC85080
  • Agency: NIDA NIH HHS, United States
    Id: HHSN271201200022C
  • Agency: Wellcome Trust, United Kingdom
    Id: 084723/Z/08/Z

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1000 Genomes Project and AWS (tool)

RRID:SCR_008801

A dataset containing the full genomic sequence of 1,700 individuals, freely available for research use. The 1000 Genomes Project is an international research effort coordinated by a consortium of 75 companies and organizations to establish the most detailed catalogue of human genetic variation. The project has grown to 200 terabytes of genomic data including DNA sequenced from more than 1,700 individuals that researchers can now access on AWS for use in disease research free of charge. The dataset containing the full genomic sequence of 1,700 individuals is now available to all via Amazon S3. The data can be found at: http://s3.amazonaws.com/1000genomes The 1000 Genomes Project aims to include the genomes of more than 2,662 individuals from 26 populations around the world, and the NIH will continue to add the remaining genome samples to the data collection this year. Public Data Sets on AWS provide a centralized repository of public data hosted on Amazon Simple Storage Service (Amazon S3). The data can be seamlessly accessed from AWS services such Amazon Elastic Compute Cloud (Amazon EC2) and Amazon Elastic MapReduce (Amazon EMR), which provide organizations with the highly scalable compute resources needed to take advantage of these large data collections. AWS is storing the public data sets at no charge to the community. Researchers pay only for the additional AWS resources they need for further processing or analysis of the data. All 200 TB of the latest 1000 Genomes Project data is available in a publicly available Amazon S3 bucket. You can access the data via simple HTTP requests, or take advantage of the AWS SDKs in languages such as Ruby, Java, Python, .NET and PHP. Researchers can use the Amazon EC2 utility computing service to dive into this data without the usual capital investment required to work with data at this scale. AWS also provides a number of orchestration and automation services to help teams make their research available to others to remix and reuse. Making the data available via a bucket in Amazon S3 also means that customers can crunch the information using Hadoop via Amazon Elastic MapReduce, and take advantage of the growing collection of tools for running bioinformatics job flows, such as CloudBurst and Crossbow.

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