Efficient Generation of Transcriptomic Profiles by Random Composite Measurements
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Abstract
RNA profiles are an informative phenotype of cellular and tissue states but can be costly to generate at massive scale. Here, we describe how gene expression levels can be efficiently acquired with random composite measurements-in which abundances are combined in a random weighted sum. We show (1) that the similarity between pairs of expression profiles can be approximated with very few composite measurements; (2) that by leveraging sparse, modular representations of gene expression, we can use random composite measurements to recover high-dimensional gene expression levels (with 100 times fewer measurements than genes); and (3) that it is possible to blindly recover gene expression from composite measurements, even without access to training data. Our results suggest new compressive modalities as a foundation for massive scaling in high-throughput measurements and new insights into the interpretation of high-dimensional data.
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A subset of expression measurements may be enough to infer many transcriptional states accurately.
“many transcriptional states could be faithfully inferred from a subset of gene expression measurements32,33”
From Combinatorial single-cell CRISPR screens by direct guide RNA capture and targeted sequencing (2020) · cites this paper as [32]
The approach is complementary to efforts based on composite measurements, compressed sensing, and rich readouts to predict unmeasured genetic interactions.
“This provides a complementary approach to efforts based on composite measurements, compressed sensing, and rich readouts to predict unmeasured GIs (7, 28).”
From Exploring genetic interaction manifolds constructed from rich single-cell phenotypes (2019) · cites this paper as [28]
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- Authors
- Cleary, B., Cong, L., Cheung, A., Lander, E. S., & Regev, A.
- Affiliations
- Broad Institute (US)
- Corresponding author
- Regev, Aviv
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2017-11
- Volume
- 171
- Issue
- 6
- Pages
- 1424-1436.e18
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC5726792
- OpenAlex
- W2768455369
- Cited by
- 114
- References
- 62
- Citations by year
- 2026: 2 · 2025: 8 · 2024: 14 · 2023: 9 · 2022: 14 · 2021: 14 · 2020: 16 · 2019: 20 · 2018: 14 · 2017: 2 · 2016: 1
- FWCI
- 5.81
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-nd)
- PMC
- Funders
- NHGRI CEGS (RM1HG006193)
- HHMI
- Klarman Cell Obervatory
- CRI
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Physical Sciences › Engineering › Computational Mechanics › Sparse and Compressive Sensing Techniques
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Keywords
- gene expression profiling, transcriptomics, compressed sensing, sparse representation, high-dimensional data
- MeSH terms
- Algorithms, Humans, Sequence Analysis, RNA, K562 Cells, Gene Expression Profiling, Data Compression, High-Throughput Nucleotide Sequencing
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