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Methods for high-throughput MethylCap-Seq data analysis

Overview of attention for article published in BMC Genomics, October 2012
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Title
Methods for high-throughput MethylCap-Seq data analysis
Published in
BMC Genomics, October 2012
DOI 10.1186/1471-2164-13-s6-s14
Pubmed ID
Authors

Benjamin AT Rodriguez, David Frankhouser, Mark Murphy, Michael Trimarchi, Hok-Hei Tam, John Curfman, Rita Huang, Michael WY Chan, Hung-Cheng Lai, Deval Parikh, Bryan Ball, Sebastian Schwind, William Blum, Guido Marcucci, Pearlly Yan, Ralf Bundschuh

Abstract

Advances in whole genome profiling have revolutionized the cancer research field, but at the same time have raised new bioinformatics challenges. For next generation sequencing (NGS), these include data storage, computational costs, sequence processing and alignment, delineating appropriate statistical measures, and data visualization. Currently there is a lack of workflows for efficient analysis of large, MethylCap-seq datasets containing multiple sample groups.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 69 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Switzerland 1 1%
Turkey 1 1%
Brazil 1 1%
United Kingdom 1 1%
Iran, Islamic Republic of 1 1%
Greece 1 1%
Luxembourg 1 1%
Unknown 62 90%

Demographic breakdown

Readers by professional status Count As %
Researcher 25 36%
Student > Ph. D. Student 9 13%
Professor > Associate Professor 7 10%
Student > Bachelor 6 9%
Student > Master 5 7%
Other 9 13%
Unknown 8 12%
Readers by discipline Count As %
Agricultural and Biological Sciences 30 43%
Biochemistry, Genetics and Molecular Biology 9 13%
Medicine and Dentistry 7 10%
Neuroscience 4 6%
Engineering 3 4%
Other 6 9%
Unknown 10 14%