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Highly sensitive and specific microRNA expression profiling using BeadArray technology

delete2008-06-25
delete103
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陈静 封面图
陈静 (Jing Chen)
J
Jean Lozach
E
Eliza Wickham Garcia
B
Bret Barnes
S
Shujun Luo
I
Ivan Mikoulitch
L
Lixin Zhou
G
Gary P. Schroth
J
Jian‐Bing Fan *
DOI:10.1093/nar/gkn387delete
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摘要

摘要

En 中文
We have developed a highly sensitive, specific and reproducible method for microRNA (miRNA) expression profiling, using the BeadArray technology. This method incorporates an enzyme-assisted specificity step, a solid-phase primer extension to distinguish between members of miRNA families. In addition, a universal PCR is used to amplify all targets prior to array hybridization. Currently, assay probes are designed to simultaneously analyse 735 well-annotated human miRNAs. Using this method, highly reproducible miRNA expression profiles were generated with 100-200 ng total RNA input. Furthermore, very similar expression profiles were obtained with total RNA and enriched small RNA species (R-2 >= 0.97). The method has a 3.5-4 log (10(5)-10(9) molecules) dynamic range and is able to detect 1.2- to 1.3-fold-differences between samples. Expression profiles generated by this method are highly comparable to those obtained with RTPCR (R-2 = 0.850.90) and direct sequencing (R = 0.870.89). This method, in conjunction with the 96-sample array matrix should prove useful for high-throughput expression profiling of miRNAs in large numbers of tissue samples.
Keyword:
MAMMALIAN MICRORNAS
IDENTIFICATION
SIGNATURES
ROLES
ARRAY
RNAS
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期刊

Nucleic Acids Research 封面图
Nucleic Acids Research
IF:
13.1
论文数:
3.6W
被引数:
29.0W

机构

I
illumina
学者数:
1.1K
论文数: 463
被引数: 1
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