How it works
In your lab
Barcode DNA from individual cells using a single cell sequencing library preparation workflow and then send your library to Loop
At Loop Genomics
We’ll barcode each transcript
Optionally enrich for target sequence using oligo pools
Sequence, assemble, and prepare a report
Case Study: EIF4A2
Using LoopSeq’s Single Cell Long-read Transcriptomics technology, we found almost all of the 27 previously identified mRNA variants of EIF4A2 and were able to determine the number of transcripts associated with each variant.
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