Statistical methods for identifying differentially expressed genes in RNA-Seq exeriments
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作者:
Fang, Zhide
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Louisiana State Univ, Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USALouisiana State Univ, Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USA
Fang, Zhide
[1
]
Martin, Jeffrey
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Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Genom Div, Berkeley, CA 94720 USA
Joint Genome Inst, Dept Energy, Walnut Creek, CA 94598 USALouisiana State Univ, Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USA
Martin, Jeffrey
[2
,3
]
Wang, Zhong
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机构:
Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Genom Div, Berkeley, CA 94720 USA
Joint Genome Inst, Dept Energy, Walnut Creek, CA 94598 USA
DOE Joint Genome Inst, Walnut Creek, CA 94598 USALouisiana State Univ, Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USA
Wang, Zhong
[2
,3
,4
]
机构:
[1] Louisiana State Univ, Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Genom Div, Berkeley, CA 94720 USA
[3] Joint Genome Inst, Dept Energy, Walnut Creek, CA 94598 USA
[4] DOE Joint Genome Inst, Walnut Creek, CA 94598 USA
RNA sequencing (RNA-Seq) is rapidly replacing microarrays for profiling gene expression with much improved accuracy and sensitivity. One of the most common questions in a typical gene profiling experiment is how to identify a set of transcripts that are differentially expressed between different experimental conditions. Some of the statistical methods developed for microarray data analysis can be applied to RNA-Seq data with or without modifications. Recently several additional methods have been developed specifically for RNA-Seq data sets. This review attempts to give an in-depth review of these statistical methods, with the goal of providing a comprehensive guide when choosing appropriate metrics for RNA-Seq statistical analyses.
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