Element 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

Request a Quote

How It Works — In Your Lab

Add Cell Barcode

Barcode DNA from individual cells using a single cell sequencing library preparation workflow and then send your library to Element Biosciences.

How It Works — At Loop Genomics

Cell Barcode to Transcript Barcode

We’ll barcode each transcript

Streptavidin-coated Bead

Optionally enrich for target sequence using oligo pools

LoopSeq report photo

Sequence, assemble, and prepare a report

Case Study: EIF4A2

mRNA variants of 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.

Ask Us About LoopSeq

Which Are You Interested In?

By submitting this form you agree to our Privacy Policy and Terms and Conditions.

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.