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 Element Biosciences.
How It Works — 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.