Testing rare variants for hypertension using family-based tests with different weighting schemes

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This paper proposes 4 weighting schemes for the family-based rare variants test (FBAT-v) to test for the effects of both rare and common variants across the genome.

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5 p.

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Wang, Xuexia; Zhao, Xingwang & Zhou, Jin October 18, 2016.

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This paper is part of the collection entitled: UNT Scholarly Works and was provided by the UNT College of Arts and Sciences to the UNT Digital Library, a digital repository hosted by the UNT Libraries. It has been viewed 37 times. More information about this paper can be viewed below.

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This paper proposes 4 weighting schemes for the family-based rare variants test (FBAT-v) to test for the effects of both rare and common variants across the genome.

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5 p.

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  • Genetic Analysis Workshop 19, August 24-26, 2016. Vienna, Austria.

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  • Publication Title: BMC Proceedings: Genetic Analysis Workshop 19: Sequence, Blood Pressure and Expression Data.
  • Volume: 10
  • Issue: Supplement 7
  • Pages: 5
  • Page Start: 233
  • Page End: 237

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  • October 18, 2016

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  • March 15, 2017, 12:42 p.m.

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  • Feb. 2, 2021, 2:58 p.m.

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Wang, Xuexia; Zhao, Xingwang & Zhou, Jin. Testing rare variants for hypertension using family-based tests with different weighting schemes, paper, October 18, 2016; London, UK. (https://digital.library.unt.edu/ark:/67531/metadc958746/: accessed May 29, 2024), University of North Texas Libraries, UNT Digital Library, https://digital.library.unt.edu; crediting UNT College of Arts and Sciences.

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