Abstract
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.
Original language | English |
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Pages (from-to) | E2183-E2192 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 115 |
Issue number | 10 |
DOIs | |
State | Published - 6 Mar 2018 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2018 National Academy of Sciences. All Rights Reserved.
Funding
ACKNOWLEDGMENTS. We thank Ninning Liu, Mingjie Dai, Thomas C. Ferrante, Josh Rosenberg, Nikhil Gopalkrishnan, Florian Schüder, Ralf Jungmann, Jesse Silverberg, Sungwook Woo, and members of the laboratories of P.Y. and C.-t.W. for helpful discussions; Jin Billy Li for the idea to use k-mer filtering as a means of specificity checking; and Geoffrey Fudenberg for assistance with the 19p13.2 probe design. This work was supported by National Institutes of Health Awards 1R01EB018659-01 (to P.Y.), 1-U01-MH106011-01 (to P.Y.), DP1GM106412 (to C.-t.W.), and R01HD091797 (to C.-t.W.); Office of Naval Research Awards N00014-13-1-0593 (to P.Y.), N00014-14-1-0610 (to P.Y.), N00014-16-1-2182 (to P.Y.), and N00014-16-1-2410 (to P.Y.); National Science Foundation (NSF) Awards CCF-1054898 and CCF-1317291 (to P.Y.); a Damon Runyon Cancer Research Foundation Fellowship (to B.J.B.); a Uehara Memorial Foundation Research Fellowship (to H.M.S.); postdoctoral fellowships from the European Molecular Biology Organization (to S.K.S.) and the Human Frontier Science Program (to S.K.S.); and NSF Graduate Research Fellowships (to J.Y.K. and S.C.N.). We thank Ninning Liu, Mingjie Dai, Thomas C. Ferrante, Josh Rosenberg, Nikhil Gopalkrishnan, Florian Schüder, Ralf Jungmann, Jesse Silverberg, Sungwook Woo, and members of the laboratories of P.Y. and C.-t.W. for helpful discussions; Jin Billy Li for the idea to use k-mer filtering as a means of specificity checking; and Geoffrey Fudenberg for assistance with the 19p13.2 probe design. This work was supported by National Institutes of Health Awards 1R01EB018659-01 (to P.Y.), 1-U01-MH106011-01 (to P.Y.), DP1GM106412 (to C.-t.W.), and R01HD091797 (to C.-t.W.); Office of Naval Research Awards N00014-13-1-0593 (to P.Y.), N00014-14-1-0610 (to P.Y.), N00014-16-1-2182 (to P.Y.), and N00014-16-1-2410 (to P.Y.); National Science Foundation (NSF) Awards CCF-1054898 and CCF-1317291 (to P.Y.); a Damon Runyon Cancer Research Foundation Fellowship (to B.J.B.); a Uehara Memorial Foundation Research Fellowship (to H.M.S.); postdoctoral fellowships from the European Molecular Biology Organization (to S.K.S.) and the Human Frontier Science Program (to S.K.S.); and NSF Graduate Research Fellowships (to J.Y.K. and S.C.N.).
Funders | Funder number |
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NSF Graduate Research Fellowships | |
National Institutes of Health Awards 1R01EB018659-01 | |
Office of Naval Research Awards N00014-13-1-0593 | |
S.C.N. | |
National Science Foundation | CCF-1317291, CCF-1054898 |
National Institutes of Health | DP1GM106412, 1R01EB018659-01, 1-U01-MH106011-01 |
Office of Naval Research | N00014-14-1-0610, N00014-16-1-2410, N00014-13-1-0593, N00014-16-1-2182 |
National Institute of Child Health and Human Development | R01HD091797 |
Damon Runyon Cancer Research Foundation | |
European Molecular Biology Organization | |
Human Frontier Science Program | |
Uehara Memorial Foundation | |
National Science Foundation |
Keywords
- FISH
- In situ
- Oligo
- Oligonucleotide
- Superresolution