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Calculation of MAX test P value with geometric characterization of 2x3 table tests

Calculation of MAX test P value with geometric characterization of 2x3 table tests. 2010 Joint Statistical Meetings Vancouver, Canada 2010/08/05 Ryo Yamada Kyoto Univ. Kyoto Japan. Case-Control x MM,Mm,mm genotypes Genetic models Dominant Recessive Somewhere between them.

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Calculation of MAX test P value with geometric characterization of 2x3 table tests

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  1. Calculation of MAX test P value with geometric characterization of 2x3 table tests 2010 Joint Statistical Meetings Vancouver, Canada 2010/08/05 Ryo Yamada Kyoto Univ. Kyoto Japan

  2. Case-ControlxMM,Mm,mm genotypesGenetic modelsDominantRecessiveSomewhere between them

  3. Contingency tables test with ellipse and sphere • N categories x M categories

  4. K categories are expressed as (K-1)-simplex or K-complete graph

  5. 3 categories in a triangle4 categories in a tetrahedronand so on

  6. NxM vectors can be placed in df-dimensional space 2x4=8 vectors 2x3=6 vectors

  7. Pearson’s chi-sq values draws ellipsoid contour lines,which can be spherized • Expected values determine shape of ellipsoid Spherization Spherization Tables on a contour line have the same statistic value

  8. Spherization = Eigenvalue decomposition Eigenvalue decomposition

  9. Any test of 1 df is a plane tangent to the ellipsoid or the sphere • Tables with the same Psn’s chi-sq are ellipsoid/sphere. • Tables with the same stat value of test of 1 df are a plane.

  10. Any test of 1 df = a vector in the space • In the spherized coordinate, the radius to the tangent point is perpendicular to the plane. • In the coordinate with ellipsoid, NOT perpendicular. a Test Vector b Tangent point to the smaller sphere.

  11. MAX3 test for 2x3 table • 3 tests of 1 df in matrix-form and vector-form • Find tangent points for three test planes. rec add dom

  12. The contour lines of MAX3 test stats arecombinations of 3 parallel line sets

  13. To which model fit most?It depends where the observed table locates. Recessive Additive Dominant Dominant Recessive Additive

  14. MAX testAny model between dominant and recessive • Two sets of parallel lines with arcs Arc

  15. P value Probability of tables with a statistic value equal to or more than the observed table

  16. Pr(θ): The probability further than the contour line in the direction

  17. How to integrate? • For 2x3 tables (df=2), • Sum of the probabilities in evenly spaced multiple directions gives the good approximation of the integral.

  18. Multiple tests of 1 df on a table with higher dimensions

  19. How to integrate? • For NxM tables (df=(N-1)x(M-1)), • Sum of the probabilities in evenly spaced multiple directions gives the good approximation of the integral.

  20. How to integrate? • For NxM tables (df=(N-1)x(M-1)), • Sum of the probabilities in evenly spaced multiple directions gives the good approximation of the integral.

  21. How to integrate? • For NxM tables (df=(N-1)x(M-1)), • Sum of the probabilities in randomly spaced multiple directions gives the good approximation of the integral.

  22. How to integrate? • For NxM tables (df=(N-1)x(M-1)), • Sum of the probabilities in randomly spaced multiple directions gives the good approximation of the integral.

  23. Random directions are easy to be sampled in the “spherized” coordinate.

  24. Random directions are easy to be sampled in the “spherized” coordinate.

  25. Random directions are easy to be sampled in the “spherized” coordinate.

  26. Random directions are easy to be sampled in the “spherized” coordinate.

  27. Random directions are easy to be sampled in the “spherized” coordinate.

  28. Random directions are easy to be sampled in the “spherized” coordinate.

  29. P-value estimation using random points on the sphere fits well with the permutation method Black : Permutation Red : Sphere method

  30. R code and web-based calculator of the method for 2x3 table presented are available at; http://www.genome.med.kyoto-u.ac.jp/wiki_tokyo/index.php/Estimate_of_P-value_of_MAX_for_2x3_tables Comments and questions are welcome → ryamada@genome.med.kyoto-u.ac.jp • Collaborators • Graduate school of Medicine, Kyoto University, Kyoto, Japan • Takahisa Kawaguchi • Katsura Hirosawa • Meiko Takahashi • Fumihiko Matsuda • Lab for Autoimmune Diseases, CGM, RIKEN, Yokohama, Japan • Yukinori Okada • Yuta Kochi • Akari Suzuki • Kazuhiko Yamamoto

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