Variant Callers for Next-Generation Sequencing Data: A Comparison Study

Open Access

Peer-reviewed

Research Article

Xiangtao Liu,

Affiliations Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America, VA CT Health Care Center, West Haven, Connecticut, United States of America
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Shizhong Han,

Affiliations Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America, VA CT Health Care Center, West Haven, Connecticut, United States of America
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Zuoheng Wang,

Affiliation Department of Biostatistics, Yale School of Public Health, New Haven, Connecticut, United States of America
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Joel Gelernter,

Affiliations Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America, VA CT Health Care Center, West Haven, Connecticut, United States of America, Departments of Genetics and Neurobiology, Yale University School of Medicine, New Haven, Connecticut, United States of America
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Bao-Zhu Yang

* E-mail: bao-zhu.yang@yale.edu

Affiliations Department of Psychiatry, Division of Human Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America, VA CT Health Care Center, West Haven, Connecticut, United States of America
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Single nucleotide polymorphisms
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Genome sequencing
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Variant genotypes
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Sequence alignment
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Dideoxy DNA sequencing
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Genomics
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Next-generation sequencing
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Genome-wide association studies
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