- More comprehensive coverage and more complete assemblies, thanks to fewer, longer contigs
- Unaffected by GC-content
- Better quality scores
- 40x lower error rates than classical Illumina workflows
LoopSeq’s Long-Read technology combines the affordability of Illumina short-read sequencing, the assembly power of a long-read approach and the unparalleled sequence accuracy that is unique to Loop Genomics.
Regardless of GC-content of Genome size, the Bacterial whole genome sequencing (WGS) kit outperforms conventional short-read workflows
LoopSeq reads assemble into 89- to 6-fold fewer contigs than PE150 reads or PE300 reads.
LoopSeq reads assemble into 89- to 6-fold fewer contigs than PE150 reads or PE300 reads.
LoopSeq assemblies average a 5.7-fold larger N50 value compared to PE150 assemblies, indicating more comprehensive genome coverage.
LoopSeq assemblies average a 5.7-fold larger N50 value compared to PE150 assemblies, indicating more comprehensive genome coverage.
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