23andme white paper
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2021 Appendix to White Paper 23-21
This appendix contains key information for models released in 2021 developed under the methods outlined in White Paper 23-21 See the appendix for 2020 here |
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A Generalized Method for the Creation and Evaluation of Polygenic
2 jui 2020 · 23andMe White Paper 23-12: · Estimating Complex Phenotype Prevalence Using Predictive Models 23andMe https://permalinks 23andme com/ pdf /23 |
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2022 Appendix to White Paper 23-21
This appendix contains key information for polygenic scores released in 2022 developed under the methods outlined in White Paper 23-21 See the appendix for |
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Appendix to White Paper 23-21
This appendix contains key information for models developed under the methods outlined in White Paper 23-21 This appendix is updated with every new report |
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White Paper 23-03
10 jui 2010 · incidence can be found in 23andMe White Paper 23-02 ) A population is only pre- sented as a choice if there is at least one SNP that passes |
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White Paper 23-17
The predictive models for BMI and gene-by-environment interactions presented in this white paper form the basis for 23andMe's Genetic Weight report Because |
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White Paper 23-19
The predictive models based on genetics use multiple genetic markers reflecting the polygenic nature of T2D Building on these promising findings and harnessing |
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White Paper 23-21
We intend for this White Paper and the Appendices to be living documents that will be updated as methodologies change and new PGS-based genetic reports are |
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2023 Appendix to White Paper 23-21
the methods outlined in White Paper 23-21 See the appendix for 2020 here 2021 here and 2022 here Contents: 1 Preeclampsia 2 Attention Deficit |
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Introduction
Genetic variants are assayed using Illumina BeadChip arrays as previously described in. 23andMe White Paper 23-19 ?(Multhaup et al. 2019)?. In summary |
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The science behind 23andMes Type 2 Diabetes report
White Paper 23-19. The science behind 23andMe's Type 2 Diabetes report. Estimating the likelihood of developing type 2 diabetes with polygenic models. |
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White Paper 23-?12 Estimating Complex Phenotype Prevalence
25 sept. 2015 23andMe White Paper 23-?12. Page 2 of 11. Introduction. In this white paper we describe an approach for creating and evaluating predictive. |
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White Paper 23-05: Neanderthal Ancestry Inference
8 juil. 2020 Scientists at 23andMe further noticed that several of these Neanderthal variants are associated with traits in 23andMe customers. This white ... |
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23andMe
White Paper 23-14. Ancestry Timeline. Authors: Katarzyna Bryc kbryc@23andme.com. Eric Y. Durand. Joanna Mountain. Created: 1 December 2016. |
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White Paper 23-17
White Paper 23-17. The science behind 23andMe's Genetic Weight report. Estimating BMI and associated phenotypes with polygenic risk models. Authors:. |
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White Paper 23-?10 Parkinsons Disease - 23andMe Blog
White Paper Summarizing Findings from the 23andMe Parkinson's. Disease Research Community. Paul Cannon PhD. Parkinson's Disease Program Manager |
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FINAL White paper 23-20 19Jun2019 - Google Docs
19 juin 2019 White Paper 2320. Standards of evidence for health and wellness recommendations. Authors: Becca Krock PhD (bkrock@23andme.com). |
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A scalable pipeline for local ancestry inference using tens of
7 déc. 2020 genetics company 23andMe |
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White Paper 23-?11
28 sept. 2015 White Paper 23-?11. Estimating Carrier Frequency Carrier Detection Rate |
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White Paper - 23andMe
White Paper 23-19 The science behind 23andMe's Type 2 Diabetes report Estimating the likelihood of developing type 2 diabetes with polygenic models |
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White Paper 23-21 - 23andMe for Medical Professionals
White Paper 23-21 A Generalized Method for the Creation and Evaluation of Polygenic Scores James R Ashenhurst*, Jianan Zhan*, Michael L Multhaup, Ryo |
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Appendix to White Paper 23-21 - PGS methods Final Draft - 23andMe
The p-values for each variant shared between the 23andMe (blue) and Global Lipids Genetics Consortium (GLGC; red) genome-wide association studies ( |
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A scalable pipeline for local ancestry inference using - 23andMe
7 déc 2020 · Abstract Ancestry deconvolution is the task of identifying the ancestral origins of chromosomal segments of admixed individuals |
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White Paper 23-‐12 Estimating Complex Phenotype - 23andMe
25 sept 2015 · 23andMe White Paper 23-‐12 Page 2 of 11 Introduction In this white paper, we describe an approach for creating and evaluating predictive |
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Summary - 23andMe
4 déc 2014 · White Paper 23-08 Genetic Associations with Traits in 23andMe Customers Authors: Saniya Fayzullina Robin P Smith Nicholas Furlotte |
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White Paper 23-‐10 Parkinsons Disease - The - 23andMe Blog
White Paper Summarizing Findings from the 23andMe Parkinson's Disease Research Community Paul Cannon, PhD Parkinson's Disease Program Manager, |
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Summary - 23andMe Blog
WhitePaper23-08 GeneticAssociationswithTraitsin23andMeCustomers new"trait"associations"to"this"white"paper"as"more"23andMe"GWAS"results" |
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White Paper 23-‐09 Analysis of &#TheDress - 23andMe Blog
23 mar 2015 · For similar traits such as color blindness, Page 2 Analysis of #TheDress in 23andMe Customers March 25, 2014 White Paper 23 -‐ 09 An |
![Cecile Janssens on Twitter: \](https://i1.rgstatic.net/publication/326494078_The_Future_is_Hypernormative_an_analysis_of_bodymind_representations_in_23andMe's_commercials/links/5b51221d45851507a7b1f68f/largepreview.png "Cecile Janssens on Twitter: \")
![23andMe confirms: I'm super white\](https://thestripe.com/wp-content/uploads/2017/07/23-and-me-1.jpg "23andMe confirms: I'm super white\")
