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Image based transcriptomics
Trace Henry
HHMI Janelia Research Campus
Aproaches for spatial genomics
https://www.youtube.com/watch?v=myx8N0zjx48&t=234s
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
reported genes
reportedcells
https://www.youtube.com/watch?v=myx8N0zjx48&t=234s
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
Moor and Itzkovitz, Current Opinion Biotech, 2017
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
Batish et al., Methods in Mol Bio, 2011
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
Spatial Barcoding w/ 

Superesolution imaging
Lubeck and Cai, Nature Methods, 2012
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
Battich et al., Nature Methods, 2013
Sequential Methods A:

1 gene = 1 color,

many rounds + stripping
# genes = F * N
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
Sequential Methods B:

Barcoding strategy,

many rounds + stripping
Lubeck et al., Nature Methods, 2014
# genes = FN
SeqFISH (2016)
Shah, Lubeck, et al., Neuron, 2016
SeqFISH Barcoding strategy
125 genes profiled, 100 of which are barcoded and 25 are identified by serial smHCR hybridizations. Five control genes (Hdx,
Vps13c, Zfp715, Fbll1, Slc4a8) were quantified by both techniques. The smHCR round of hybridization of control genes were
performed twice to colocalize signal to obtain an absolute count.
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
B-actin
MAP2
Merfish
MERFISH (2015)
“multiplexed error-robust
fluorescence in situ hybridization”
Encoding Scheme 1
• 16 bit barcodes

• ID 140 unique mRNA species

• 80% detection efficiency

• ~100 human fibroblast cells

in single 18Hr period
Chen, Boettiger, et al., Science, 2015
MERFISH v2 (2016)
~15,000 cells
• Much faster than previous version

• 40K cells in 18Hr period

• 3 major changes:

1. No photobleaching

2. Larger FOV

3. Two color imaging
Moffitt, Hao, Wang, et al., PNAS, 2016
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
Multiplexed ion beam imaging
Angelo et al., Nature Medicine, 2014
Direct Measurement
multiplex

RNA fISH
in situ multi-

plex protein 

localization
In situ 

sequencing
Aproaches for spatial genomics
Moor and Itzkovitz, Current Opinion Biotech, 2017
mRNA —> cDNA —> Nanoballs (via RCA)
Targeted 

via Padlock 

probes (ISS)
Unbiased 

via random 

hexamers (FISSEQ)
In situ sequencing
(Nillsson)
Uses padlock probes to target specific mRNAs, with cDNA synthesis
and rolling-circle amplification in situ, followed by sequencing by ligation
Ke, et al., Nature Methods, 2013
Fisseq (2014) “Fluorescent in situ sequencing”
(6) 3D in situ RNA sequencing library within the cell
(1) A tagged random hexamer primer is used to prime
reverse transcriptase to generate modified cDNA
fragments in fixed cells or tissues.
(2) BS(PEG)9 permanently cross-links the modified
cDNA and the cellular protein matrix.
(3) cDNA circularization
(4) DNA polymerase generates cDNA amplicons
(5) amplicons are cosslinked
Lee, et al., Science, 2014
Fisseq (2014): SOLID based sequencing
- Each amplicon contains numerous tandem copies of the cDNA template and adapter
sequence.
- A sequencing primer hybridizes to the adapter sequences in individual amplicons, and
fluorescent eight-base probes interrogate the adjacent dinucleotide pair.
- After imaging, the three bases attached to a fluorophore are cleaved, generating a
phosphorylated 5′ end at the ligation complex suitable for additional ligation cycles
interrogating every fifth dinucleotide pairs.
- The whole process is repeated using four other sequencing primers with an offset to
interrogate intervening base positions
Lee, et al., Nature Protocols, 2015
Fisseq (2014): Technical considerations
Extending sequencing primers by one or more bases,
one can randomly sample amplicons at 1/4th, 1/16th,
and 1/256th of the original density in fibroblasts
Due to the size of the generated Nano balls
(200-400nm) and technical limitations of optics, only a
few hundred molecules can be detected in each cell
Also, efficiency of RCA is not uniform across
subcellular compartments, especially across different
cell types
Sensitivity of padlock probes is two orders of magnitude
higher than FISSEQ for a given gene
Lee, et al., Science, 2014
Fisseq (2014)
Lee, et al., Science, 2014
Inference
Computational Imputation
Aproaches for spatial genomics
Habib, Li, et al., Science, 2016
Inference
Computational Imputation
Aproaches for spatial genomics
Satija et al., Nature Biotechnology, 2015
Gridding/Barcoding Inference Direct Measurement
“Spatial Transcriptomics”
multiplex

RNA fISH
in situ multi-

plex protein 

localization
Computational Imputation
In situ 

sequencing
Aproaches for spatial genomics
1) Tissue Fixation on slide 2) Permeabilization
3) cDNA Synthesis
4) Library Prep and Sequencing
Stahl, Salmen, et al., Science 2016
Stahl, Salmen, et al., Science 2016
“Spatial Transcriptomics”
Commercially Available!
Croesetto, et al., Nat Rev Genetics ,2015
Grand Overview
Things to consider: What genes to pick?
Tasic, Menon, et al., Nature Neuroscience, 2016
How to overcoming crowding issue: Expansion Microscopy
Chen, Wassie, et al., Nature Methods, 2016
How to overcoming crowding issue: Correlation decoding
Coskun and Cai, Nature Methods, 2016
https://github.com/chanzuckerberg/starfish
Hypothetical Analysis Pipeline
Spatial DE: Identification of spatially variable genes
https://www.biorxiv.org/content/early/2017/05/28/143321
Applications to neuroscience
Lein, et al., Science, 2017
END

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Image Based Transcriptomics: An Overview

  • 1. Image based transcriptomics Trace Henry HHMI Janelia Research Campus
  • 2. Aproaches for spatial genomics https://www.youtube.com/watch?v=myx8N0zjx48&t=234s
  • 3. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 reported genes reportedcells https://www.youtube.com/watch?v=myx8N0zjx48&t=234s
  • 4. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics Moor and Itzkovitz, Current Opinion Biotech, 2017
  • 5. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 Batish et al., Methods in Mol Bio, 2011
  • 6. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 Spatial Barcoding w/ Superesolution imaging Lubeck and Cai, Nature Methods, 2012
  • 7. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 Battich et al., Nature Methods, 2013 Sequential Methods A: 1 gene = 1 color, many rounds + stripping # genes = F * N
  • 8. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 Sequential Methods B: Barcoding strategy, many rounds + stripping Lubeck et al., Nature Methods, 2014 # genes = FN
  • 9. SeqFISH (2016) Shah, Lubeck, et al., Neuron, 2016
  • 10. SeqFISH Barcoding strategy 125 genes profiled, 100 of which are barcoded and 25 are identified by serial smHCR hybridizations. Five control genes (Hdx, Vps13c, Zfp715, Fbll1, Slc4a8) were quantified by both techniques. The smHCR round of hybridization of control genes were performed twice to colocalize signal to obtain an absolute count.
  • 11. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics B-actin MAP2 Merfish
  • 12. MERFISH (2015) “multiplexed error-robust fluorescence in situ hybridization” Encoding Scheme 1 • 16 bit barcodes • ID 140 unique mRNA species • 80% detection efficiency • ~100 human fibroblast cells in single 18Hr period Chen, Boettiger, et al., Science, 2015
  • 13. MERFISH v2 (2016) ~15,000 cells • Much faster than previous version • 40K cells in 18Hr period • 3 major changes: 1. No photobleaching 2. Larger FOV 3. Two color imaging Moffitt, Hao, Wang, et al., PNAS, 2016
  • 14. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics Multiplexed ion beam imaging Angelo et al., Nature Medicine, 2014
  • 15. Direct Measurement multiplex RNA fISH in situ multi- plex protein localization In situ sequencing Aproaches for spatial genomics Moor and Itzkovitz, Current Opinion Biotech, 2017 mRNA —> cDNA —> Nanoballs (via RCA) Targeted via Padlock probes (ISS) Unbiased via random hexamers (FISSEQ)
  • 16. In situ sequencing (Nillsson) Uses padlock probes to target specific mRNAs, with cDNA synthesis and rolling-circle amplification in situ, followed by sequencing by ligation Ke, et al., Nature Methods, 2013
  • 17. Fisseq (2014) “Fluorescent in situ sequencing” (6) 3D in situ RNA sequencing library within the cell (1) A tagged random hexamer primer is used to prime reverse transcriptase to generate modified cDNA fragments in fixed cells or tissues. (2) BS(PEG)9 permanently cross-links the modified cDNA and the cellular protein matrix. (3) cDNA circularization (4) DNA polymerase generates cDNA amplicons (5) amplicons are cosslinked Lee, et al., Science, 2014
  • 18. Fisseq (2014): SOLID based sequencing - Each amplicon contains numerous tandem copies of the cDNA template and adapter sequence. - A sequencing primer hybridizes to the adapter sequences in individual amplicons, and fluorescent eight-base probes interrogate the adjacent dinucleotide pair. - After imaging, the three bases attached to a fluorophore are cleaved, generating a phosphorylated 5′ end at the ligation complex suitable for additional ligation cycles interrogating every fifth dinucleotide pairs. - The whole process is repeated using four other sequencing primers with an offset to interrogate intervening base positions Lee, et al., Nature Protocols, 2015
  • 19. Fisseq (2014): Technical considerations Extending sequencing primers by one or more bases, one can randomly sample amplicons at 1/4th, 1/16th, and 1/256th of the original density in fibroblasts Due to the size of the generated Nano balls (200-400nm) and technical limitations of optics, only a few hundred molecules can be detected in each cell Also, efficiency of RCA is not uniform across subcellular compartments, especially across different cell types Sensitivity of padlock probes is two orders of magnitude higher than FISSEQ for a given gene Lee, et al., Science, 2014
  • 20. Fisseq (2014) Lee, et al., Science, 2014
  • 21. Inference Computational Imputation Aproaches for spatial genomics Habib, Li, et al., Science, 2016
  • 22. Inference Computational Imputation Aproaches for spatial genomics Satija et al., Nature Biotechnology, 2015
  • 23. Gridding/Barcoding Inference Direct Measurement “Spatial Transcriptomics” multiplex RNA fISH in situ multi- plex protein localization Computational Imputation In situ sequencing Aproaches for spatial genomics 1) Tissue Fixation on slide 2) Permeabilization 3) cDNA Synthesis 4) Library Prep and Sequencing Stahl, Salmen, et al., Science 2016
  • 24. Stahl, Salmen, et al., Science 2016 “Spatial Transcriptomics”
  • 26. Croesetto, et al., Nat Rev Genetics ,2015 Grand Overview
  • 27. Things to consider: What genes to pick? Tasic, Menon, et al., Nature Neuroscience, 2016
  • 28. How to overcoming crowding issue: Expansion Microscopy Chen, Wassie, et al., Nature Methods, 2016
  • 29. How to overcoming crowding issue: Correlation decoding Coskun and Cai, Nature Methods, 2016
  • 31. Spatial DE: Identification of spatially variable genes https://www.biorxiv.org/content/early/2017/05/28/143321
  • 32. Applications to neuroscience Lein, et al., Science, 2017
  • 33. END