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
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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

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At Loop Genomics

We’ll barcode each transcript

Optionally enrich for target sequence using oligo pools

Sequence, assemble, and prepare a report

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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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