Bi-PROF Bisulfite profiling of target regions using 454 GS FLX Titanium technology

被引:32
|
作者
Gries, Jasmin [1 ]
Schumacher, Dirk [2 ]
Arand, Julia [1 ]
Lutsik, Pavlo [1 ]
Markelova, Maria Rivera [3 ]
Fichtner, Iduna [3 ]
Walter, Joern [1 ]
Sers, Christine [2 ]
Tierling, Sascha [1 ]
机构
[1] Univ Saarland, Dept Genet Epigenet, Life Sci FR8 3, D-66123 Saarbrucken, Germany
[2] Charite, Inst Pathol, D-13353 Berlin, Germany
[3] Max Delbruck Ctr Mol Med, Berlin, Germany
关键词
DNA methylation; bisulfite profiling; next-generation sequencing; BiQ Analyzer HT; colorectal cancer; DNA METHYLATION;
D O I
10.4161/epi.25242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of next generation sequencing has expanded our view on whole mammalian methylome patterns. In particular, it provides a genome-wide insight of local DNA methylation diversity at single nucleotide level and enables the examination of single chromosome sequence sections at a sufficient statistical power. We describe a bisulfite-based sequence profiling pipeline, Bi-PROF, which is based on the 454 GS-FLX Titanium technology that allows to obtain up to one million sequence stretches at single base pair resolution without laborious subcloning. To illustrate the performance of the experimental workflow connected to a bioinformatics program pipeline (BiQ Analyzer HT) we present a test analysis set of 68 different epigenetic marker regions (amplicons) in five individual patient-derived xenograft tissue samples of colorectal cancer and one healthy colon epithelium sample as a control. After the 454 GS-FLX Titanium run, sequence read processing and sample decoding, the obtained alignments are quality controlled and statistically evaluated. Comprehensive methylation pattern interpretation (profiling) assessed by analyzing 10(2)-10(4) sequence reads per amplicon allows an unprecedented deep view on pattern formation and methylation marker heterogeneity in tissues concerned by complex diseases like cancer.
引用
收藏
页码:765 / 771
页数:7
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