LoopSeq Single Cell Long-read Transcriptomics Service

Detect and measure the abundance of splice variants, gene fusions, and novel isoforms for deeper insights into cancer and more

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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