Decoding randomly ordered DNA arrays

被引:210
作者
Gunderson, KL
Kruglyak, S
Graige, MS
Garcia, F
Kermani, BG
Zhao, CF
Che, DP
Dickinson, T
Wickham, E
Bierle, J
Doucet, D
Milewski, M
Yang, R
Siegmund, C
Haas, J
Zhou, LX
Oliphant, A
Fan, JB
Barnard, S
Chee, MS [1 ]
机构
[1] Illumina Inc, San Diego, CA 92121 USA
[2] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
关键词
D O I
10.1101/gr.2255804
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
We have developed a simple and efficient algorithm to identify each member of a large collection of DNA-linked objects through the use of hybridization, and have applied it to the manufacture of randomly assembled arrays of beads in wells. Once the algorithm has been used to determine the identity of each bead, the microarray can be used in a wide variety of applications, including single nucleotide polymorphism genotyping and gene expression profiling. The algorithm requires only a few labels and several sequential hybridizations to identify thousands of different DNA sequences with great accuracy. We have decoded tens of thousands of arrays, each with 1520 sequences represented at similar to30-fold redundancy by up to similar to50,000 beads, with a median error rate of <1 x 10(-4) per bead. The approach makes use of error checking codes and provides, for the first time, a direct functional quality control of every element of each array that is manufactured. The algorithm can be applied to any spatially fixed collection of objects or molecules that are associated with specific DNA sequences.
引用
收藏
页码:870 / 877
页数:8
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