Directional false discovery rate control in large-scale multiple comparisons
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作者:
Liang, Wenjuan
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East China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
Huangshan Univ, Sch Math & Stat, Huangshan, Peoples R ChinaEast China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
Liang, Wenjuan
[1
,2
]
Xiang, Dongdong
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机构:
East China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R ChinaEast China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
Xiang, Dongdong
[1
]
Mei, Yajun
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机构:
Georgia Inst Technol, Sch Ind & Syst Engn, Atlanta, GA USAEast China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
Mei, Yajun
[3
]
Li, Wendong
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East China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
3663 North Zhongshan Rd, Shanghai 200062, Peoples R ChinaEast China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
Li, Wendong
[1
,4
]
机构:
[1] East China Normal Univ, Sch Stat, KLATASDS MOE, Shanghai, Peoples R China
[2] Huangshan Univ, Sch Math & Stat, Huangshan, Peoples R China
[3] Georgia Inst Technol, Sch Ind & Syst Engn, Atlanta, GA USA
[4] 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China
The advance of high-throughput biomedical technology makes it possible to access massive measurements of gene expression levels. An important statistical issue is identifying both under-expressed and over-expressed genes for a disease. Most existing multiple-testing procedures focus on selecting only the non-null or significant genes without further identifying their expression type. Only limited methods are designed for the directional problem, and yet they fail to separately control the numbers of falsely discovered over-expressed and under-expressed genes with only a unified index combining all the false discoveries. In this paper, based on a three-classification multiple testing framework, we propose a practical data-driven procedure to control separately the two directions of false discoveries. The proposed procedure is theoretically valid and optimal in the sense that it maximizes the expected number of true discoveries while controlling the false discovery rates for under-expressed and over-expressed genes simultaneously. The procedure allows different nominal levels for the two directions, exhibiting high flexibility in practice. Extensive numerical results and analysis of two large-scale genomic datasets show the effectiveness of our procedure.
机构:
Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Abramovich, Felix
Benjamini, Yoav
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机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Benjamini, Yoav
Donoho, David L.
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机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Donoho, David L.
Johnstone, Iain M.
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机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
机构:
Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Abramovich, Felix
Benjamini, Yoav
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h-index: 0
机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Benjamini, Yoav
Donoho, David L.
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h-index: 0
机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel
Donoho, David L.
Johnstone, Iain M.
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h-index: 0
机构:Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, Sch Math Sci, IL-69978 Tel Aviv, Israel