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MOESM5 of “Gap hunting” to characterize clustered probe signals in Illumina methylation array data

By Shan Andrews (3504926), Christine Ladd-Acosta (86370), Andrew Feinberg (242567), Kasper Hansen (227413) and M. Fallin (3504923)

Abstract

Additional file 5: Figures S3–S25. All Remaining C and G site scenarios for Type II and Type I probes. Each additional scenario of a C and G site-mapping SNP delimited in Fig. 2 not including the scenario show in Fig. 3. Each of these figures contains the same panels (a–d) as seen in Fig. 3. All scenarios demonstrate the expected behavior shown in Fig. 2

Topics: Medicine, Genetics, Molecular Biology, Developmental Biology, Cancer, Science Policy, Infectious Diseases, Computational Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Illumina HumanMethylation450 BeadChip, 450k Array, Gap hunting, SNP, Polymorphic CpG, Epigenome-wide association studies
Year: 2016
DOI identifier: 10.6084/m9.figshare.c.3623231_d8.v1
OAI identifier: oai:figshare.com:article/4400603
Provided by: FigShare
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