OligoMiner provides a rapid, flexible environment for the design of genome-scale oligonucleotide in situ hybridization probes

被引:151
作者
Beliveau, Brian J. [1 ,2 ]
Kishi, Jocelyn Y. [1 ,2 ]
Nir, Guy [3 ]
Sasaki, Hiroshi M. [1 ,2 ]
Saka, Sinem K. [1 ,2 ]
Nguyen, Son C. [3 ,4 ]
Wu, Chao-ting [3 ]
Yin, Peng [1 ,2 ]
机构
[1] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Syst Biol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[4] Univ Penn, Dept Genet, Philadelphia, PA 19104 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
oligonucleotide; FISH; in situ; superresolution; oligo; SINGLE-MOLECULE LOCALIZATION; SUPERRESOLUTION MICROSCOPY; SPATIAL-ORGANIZATION; READ ALIGNMENT; DNA-SEQUENCES; RNA; ACID; GENE; CELLS; FISH;
D O I
10.1073/pnas.1714530115
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oligonucleotide (oligo)-based FISH has emerged as an important tool for the study of chromosome organization and gene expression and has been empowered by the commercial availability of highly complex pools of oligos. However, a dedicated bioinformatic design utility has yet to be created specifically for the purpose of identifying optimal oligo FISH probe sequences on the genome-wide scale. Here, we introduce OligoMiner, a rapid and robust computational pipeline for the genome-scale design of oligo FISH probes that affords the scientist exact control over the parameters of each probe. Our streamlined method uses standard bioinformatic file formats, allowing users to seamlessly integrate new and existing utilities into the pipeline as desired, and introduces a method for evaluating the specificity of each probe molecule that connects simulated hybridization energetics to rapidly generated sequence alignments using supervised machine learning. We demonstrate the scalability of our approach by performing genome-scale probe discovery in numerous model organism genomes and showcase the performance of the resulting probes with diffraction-limited and single-molecule superresolution imaging of chromosomal and RNA targets. We anticipate that this pipeline will make the FISH probe design process much more accessible and will more broadly facilitate the design of pools of hybridization probes for a variety of applications.
引用
收藏
页码:E2183 / E2192
页数:10
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