TY - JOUR
T1 - Intracellular spatial transcriptomic analysis toolkit (InSTAnT)
AU - Kumar, Anurendra
AU - Schrader, Alex W.
AU - Aggarwal, Bhavay
AU - Boroojeny, Ali Ebrahimpour
AU - Asadian, Marisa
AU - Lee, Ju Yeon
AU - Song, You Jin
AU - Zhao, Sihai Dave
AU - Han, Hee Sun
AU - Sinha, Saurabh
N1 - We thank Dr. Jeffrey Moffitt for sharing the data from Moffit et al.35, Zijun Wu for assistance in formatting of figures, Alton S. Barbehenn for helpful discussion for the statistical analysis, Prof. Prasanth V. Kannanganattu for advice on sample preparation. Funding: This work was supported by the National Institutes of Health (R35GM131819 to S.S., R35GM147420 to H.-S.H and A.W.S, R21HG013180 to SDZ, and T32- 842 GM136629 to M.A.), Johnson & Johnson (WiSTEM2D Award for Science to H.-S.H.), Cancer Center at Illinois (Seed grant to H.-S.H), and Georgia Institute of Technology (Wallace H. Coulter Distinguished Faculty Chair: S.S.) Facilities: We acknowledge Core Facilities at the Carl R. Woese Institute for Genomic Biology for their microscope and staff support.
We thank Dr. Jeffrey Moffitt for sharing the data from Moffit et al., Zijun Wu for assistance in formatting of figures, Alton S. Barbehenn for helpful discussion for the statistical analysis, Prof. Prasanth V. Kannanganattu for advice on sample preparation. Funding: This work was supported by the National Institutes of Health (R35GM131819 to S.S., R35GM147420 to H.-S.H and A.W.S, R21HG013180 to SDZ, and T32- 842 GM136629 to M.A.), Johnson & Johnson (WiSTEM2D Award for Science to H.-S.H.), Cancer Center at Illinois (Seed grant to H.-S.H), and Georgia Institute of Technology (Wallace H. Coulter Distinguished Faculty Chair: S.S.) Facilities: We acknowledge Core Facilities at the Carl R. Woese Institute for Genomic Biology for their microscope and staff support.
PY - 2024/12
Y1 - 2024/12
N2 - Imaging-based spatial transcriptomics technologies such as Multiplexed error-robust fluorescence in situ hybridization (MERFISH) can capture cellular processes in unparalleled detail. However, rigorous and robust analytical tools are needed to unlock their full potential for discovering subcellular biological patterns. We present Intracellular Spatial Transcriptomic Analysis Toolkit (InSTAnT), a computational toolkit for extracting molecular relationships from spatial transcriptomics data at single molecule resolution. InSTAnT employs specialized statistical tests and algorithms to detect gene pairs and modules exhibiting intriguing patterns of co-localization, both within individual cells and across the cellular landscape. We showcase the toolkit on five different datasets representing two different cell lines, two brain structures, two species, and three different technologies. We perform rigorous statistical assessment of discovered co-localization patterns, find supporting evidence from databases and RNA interactions, and identify associated subcellular domains. We uncover several cell type and region-specific gene co-localizations within the brain. Intra-cellular spatial patterns discovered by InSTAnT mirror diverse molecular relationships, including RNA interactions and shared sub-cellular localization or function, providing a rich compendium of testable hypotheses regarding molecular functions.
AB - Imaging-based spatial transcriptomics technologies such as Multiplexed error-robust fluorescence in situ hybridization (MERFISH) can capture cellular processes in unparalleled detail. However, rigorous and robust analytical tools are needed to unlock their full potential for discovering subcellular biological patterns. We present Intracellular Spatial Transcriptomic Analysis Toolkit (InSTAnT), a computational toolkit for extracting molecular relationships from spatial transcriptomics data at single molecule resolution. InSTAnT employs specialized statistical tests and algorithms to detect gene pairs and modules exhibiting intriguing patterns of co-localization, both within individual cells and across the cellular landscape. We showcase the toolkit on five different datasets representing two different cell lines, two brain structures, two species, and three different technologies. We perform rigorous statistical assessment of discovered co-localization patterns, find supporting evidence from databases and RNA interactions, and identify associated subcellular domains. We uncover several cell type and region-specific gene co-localizations within the brain. Intra-cellular spatial patterns discovered by InSTAnT mirror diverse molecular relationships, including RNA interactions and shared sub-cellular localization or function, providing a rich compendium of testable hypotheses regarding molecular functions.
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UR - http://www.scopus.com/inward/citedby.url?scp=85203286277&partnerID=8YFLogxK
U2 - 10.1038/s41467-024-49457-w
DO - 10.1038/s41467-024-49457-w
M3 - Article
C2 - 39242579
AN - SCOPUS:85203286277
SN - 2041-1723
VL - 15
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 7794
ER -