NEW - PacBio 101-986-400 Sequel Ile HiFi DNA Sequencing System

Description

Brand new system still in the unopened manufacturer's original shipping crate.
NEW - Pacific Biosciences 101-986-400 Sequel Ile HiFi DNA Sequencing System
The standard-setting Sequel IIe and Sequel II systems deliver:
Direct access to the only highly accurate long reads: PacBio HiFi reads
5-base genome sequencing (A, T, G, C, 5mC) in native DNA, for immediate access to the epigenome with no special workflow or data processing steps
Deeper biological insights, less data processing, and faster results thanks to the exceptional clarity of HiFi reads
Reliable and affordable high-throughput sequencing for a broad range of applications
For next generation sequencing, the PacBio Sequel IIe offers single molecule real-time (SMRT), long-read, DNA sequencing technology on at large though flexible scale. This platform is suitable for large scale projects such as de-novo sequencing of large and complex (plant) genomes, full length transcriptome analysis (Isoseq) large amplicon sequencing, as well as structural varian detection and haplotype phasing.
The Sequel IIe system offers the ability to run multiple chips (SMRT cells) allowing flexible on-demand sequencing, using variable sequencing run time per SMRT cell analysis. Users deploy multiple flow cells as well as variable run times (up to 30 Hours) onto single experiments for greater speed or throughput resulting in high quality long read sequences (HiFi reads).
The performance of SMRT sequencing – each Sequel IIe SMRT Cells now allows up to 8 Million ZMW wells to be loaded for sequencing simultaneous.
Technical details
Variable, up to 30 hour run time per SMRT cell
Each Sequel IIe SMRT cell has ~ eight times the sequencing capacity of a Sequel SMRT cell
8M wells per SMRT cell resulting typically in more than 5M reads
As much as 150 Gb per flow cell
Read lengths are determined by your sample and experimental needs
High Quality per base (<1% error rate) in HiFi reads, therefore making assembly, structural variation detection and phasing much more reliable, easier and faster.
Sequel IIe sequences (native) DNA — meaning no amplification bias and retained modification information
Applications
De-novo sequencing of large genomes
Structural variation analysis
Haplotype phasing
Full length transcriptome sequencing (isoSeq)
DNA modifications
Shipping
Shipping cost:
Shipped USPS or UPS and Freight for larger items.
Delivery time:
2-3 Business Days
Payment
We accept the following payment methods:
All eBay approved payments.
Please contact us if you have any questions.
Service
Quick Turnaround