This kit is for de novo bacterial genome sequencing and assembly or to deliver a comprehensive metagenomics survey and accurate relative abundance of many molecules in DNA samples. Single molecule long read data is generated as well as relative abundance using barcode based molecular counting. It also features a multiplex workflow that pools 24 samples into a single tube with less than 3 hours of hands-on time.
It’s the perfect kit for labs looking to perform de novo bacterial genome assembly or for labs looking to get long-read Metagenomics data from any DNA samples they have.
Compatible with all Illumina instruments.*
*HiSeqs, NextSeqs, and NovaSeqs are recommended for per base cost benefits.
Mechanism of Action
Synthetic long read sequencing
Allows for 24 samples to be processed in one tube
10 ng genomic DNA (2 ng/ul)
any linear dsDNA input
HiSeq 2500, HiSeq 3000, HiSeq 4000, NextSeq, NovaSeq, MiniSeq, MiSeq
Nucleic Acid Type
2 x 150 Paired End (PE) sequencing
Specialized Sample Types
PCR products, genomes, metagenomes, synthetic DNA libraries, viruses
Assembly of a synthetic long reads form short reads
The advantages of long-read sequencing. the convenience
of your existing sequencing infrastructure
Next generation sequencing (NGS) has been an incredibly powerful technique, but there
are many applications where short-read sequencing comes up, well, short.
Fortunately, Loop Genomics has developed an affordable