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Whole Genome NGS Sequencing Services


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.

• Choose isoform discovery, transcript abundance measurement, or both
• 40x lower error when compared to Illumina library prep, 7,500x lower error when compared to PacBio
• Cost-effective
• Fast turnaround


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
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Optionally enrich for target sequence using oligo pools
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Sequence, assemble, and prepare a report
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Service Description
We will use our LoopSeq single-molecule counting long-read sequencing technology for Transcriptome sequencing of your single-cell samples. Unlike RNA-seq which only counts transcripts we will not only provide transcript counting results but also unique isoform detection, enabled by our long-read technology.





Related Links

Contact us for a quote

 

 

Description Cat# Size Price    
LoopSeq Small Genome Sequencing and Assembly Service (up to 4Mb) SM_GASMSVC-LGE 1 service please inquire € DETAILS   Add to Cart 
LoopSeq Small Genome Sequencing and Assembly Service (5 to 10Mb) SM2_GASMSVC-LGE 1 service please inquire € DETAILS   Add to Cart 
LoopSeq Medium Genome Sequencing and Assembly Service (11-50 Mb) M_GASMSVC-LGE 1 service please inquire € DETAILS   Add to Cart 
LoopSeq Medium Genome Sequencing and Assembly Service (51-100 Mb) L_GASMSVC-LGE 1 service please inquire € DETAILS   Add to Cart 

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