Next Generation Sequencing (NGS) is the latest high throughput
technology to revolutionize genomic research. NGS generates massive
genomic datasets that play a key role in the big data phenomenon
that surrounds us today. To extract signals from high-dimensional
NGS data and make valid statistical inferences and predictions,
novel data analytic and statistical techniques are needed. This
book contains 20 chapters written by prominent statisticians
working with NGS data. The topics range from basic preprocessing
and analysis with NGS data to more complex genomic applications
such as copy number variation and isoform expression detection.
Research statisticians who want to learn about this growing and
exciting area will find this book useful. In addition, many
chapters from this book could be included in graduate-level classes
in statistical bioinformatics for training future biostatisticians
who will be expected to deal with genomic data in basic biomedical
research, genomic clinical trials and personalized medicine.
About the editors:
Somnath Datta is Professor and Vice Chair of Bioinformatics and
Biostatistics at the University of Louisville. He is Fellow of the
American Statistical Association, Fellow of the Institute of
Mathematical Statistics and Elected Member of the International
Statistical Institute. He has contributed to numerous research
areas in Statistics, Biostatistics and Bioinformatics.
Dan Nettleton is Professor and Laurence H. Baker Endowed Chair
of Biological Statistics in the Department of Statistics at Iowa
State University. He is Fellow of the American Statistical
Association and has published research on a variety of topics in
statistics, biology and bioinformatics."
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