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Project: PRJNA655419

RNA binding proteins (RBPs) are critical regulators of gene expression and RNA processing that are required for gene function. Yet, the dynamics of RBP regulation in single cells is unknown. To address this gap in understanding, we developed STAMP (Surveying Targets by APOBEC Mediated Profiling), which efficiently detects RBP RNA interactions. STAMP does not rely on UV crosslinking or immunoprecipitation and, when coupled with single cell capture, can identify RBP and cell type specific RNA protein interactions for multiple RBPs and cell types in single pooled experiments. Pairing STAMP with long read sequencing also yields RBP target sites for full length isoforms. Finally, conducting STAMP using small ribosomal subunits (RiboSTAMP) allows analysis of transcriptome wide ribosome association in single cells. STAMP enables the study of RBP RNA interactomes and translational landscapes with unprecedented cellular resolution. Overall design: Crosslinking and immunoprecipitation of TIA1 bound RNA and sequencing from 2 technical replicates.

Secondary Study Accession:
SRP276058
Study Title:
Robust single-cell discovery of RNA targets of RNA binding proteins and ribosomes [tia1_eclip]
Center Name:
UCSD
Study Name:
Robust single-cell discovery of RNA targets of RNA binding proteins and ribosomes [tia1_eclip]
ENA-REFSEQ:
N
PROJECT-ID:
655419
ENA-FIRST-PUBLIC:
2021-05-10
ENA-LAST-UPDATE:
2025-02-24

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PRJNA655414 Robust single-cell discovery of RNA targets of RNA binding proteins and ribosomes
RNA binding proteins (RBPs) are critical regulators of gene expression and RNA processing that are r... See more
PRJNA9558 Human genome projects have generated an unprecedented amount of knowledge about human genetics and h... See more
Study of the human condition such as genetic and infectious disease, the intersection between geneti... See more
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