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Authors
Biao Li, Baylor College of Medicine
Gao Wang, Baylor College of Medicine
Suzanne M. Leal, Baylor College of Medicine
Acknowledgment
Development of PhenoMan was supported by the NHLBI Exome Sequencing Project, the Minority Health GRID project, and the Centers for Mendelian Genomics.
Introduction
Recently, the next generation sequencing and other high-throughput technology advances to promote great interest in detecting associations between complex phenotypic traits and genetic variants. Phenotype quality control procedure is crucial and could be a complicated issue that can largely impact association analysis results. Although various decisions are likely to be made on different traits, there is lacking a simple, effective and uniformed wa
