Webinars and Sponsored Roundtables — Register Now

Tuesday, April 28, 2026, 12:00 PM–1:00 PM ET
Discover how next-day comprehensive genomic profiling (CGP) is possible with the Oncomine Comprehensive Assay Plus on the Genexus System—delivering both speed and accuracy.

Webinar presenters Jane Bayani, MHSc, PhD, Assistant Professor and Co-Director, Diagnostic Development, Ontario Institute for Cancer Research, Canada, and Nicola Normanno, MD, Scientific Director, IRCCS Romagnolo Institute for the Study of Tumors, Italy, and Morten Grauslund, PhD, Molecular Biologist, Department of Pathology, Rigshospitalet/Copenhagen University Hospital, Copenhagen, Denmark.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Thermo Fisher Scientific. For Research Use Only. Not for use in diagnostic applications. 

Thursday, April 30, 2026, 11:00 AM–12:00 PM ET
Hear an expert discuss how Memorial Sloan Kettering Cancer Center (MSKCC) is utilizing
the oncoReveal® Nexus 21-gene panel to redefine turnaround time and actionable insights
in cancer care. Dr. Ewalt shares a perceptive look at the clinical need for rapid, front-line NGS sequencing, and how a unique, purpose built targeted NGS panel (Pillar Biosciences’ oncoReveal Nexus 21 gene Panel) was developed, validated and implemented clinically by Memorial Sloan Kettering Cancer Center (MSK-REACT) to complement their current comprehensive genomic profiling (CGP) approach.

Webinar presenter Mark Ewalt, MD, Associate Medical Director for Laboratory Operations for Diagnostic Molecular Pathology in the Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, MSKCC.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Pillar Biosciences.

Thursday, May 28, 2026, 1:00–2:00 PM ET
This session is designed to improve understanding and application of recent updates to synoptic pathology reporting protocols such as the latest Reporting Template for Reporting Results of Biomarker Testing of Specimens from Patients with Carcinoma of the Breast. These changes reflect evolving clinical guidelines that directly influence diagnostic accuracy and treatment selection in breast cancer care.

Webinar presenters Thaer Khoury, MD, FCAP, Chair, Pathology and Laboratory Medicine, Roswell Park Comprehensive Cancer Cente, and Colin Murphy,  CEO of mTuitive.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Product Spotlight

Illumina

NovaSeq 6000

Company

Illumina

Name of system

NovaSeq 6000

Email

[email protected]

City, State

San Diego, CA

Phone

858-202-4500

Website

https://www.illumina.com

System application/FDA cleared or approved

research use/not required

Country where designed/Manufactured

U.S./U.S.

First year sold in U.S./First year installed in U.S.

2017/2017

System sold internationally

yes (worldwide)

Dimensions of sequencer (H × W × D)/Footprint of sequencer

65.2 × 31.5 × 37.2 in./8.2 sq. ft.

Accessory equipment supplied with sequencer at no cost

Type of computer supplied with sequencer

operating computer

Analysis options provided with sequencer

cloud based

Where library preparation is performed

wet bench

Bioinformatics tools provided with sequencer

cloud based

Sequencer supplied with UPS (uninterruptible power supply)

yes (no extra charge)

Electrical connection required for sequencer

200–240 VAC at 50/60 Hz

List price of entire sequencer and necessary components

$985,000

Purchase options

purchase, trade in, lease, reagent rental

Warranties offered

first year included with purchase; extended warranty available

Training included/Total time for basic training per operator

yes/2 days

Training location/Follow-up training available

at customer site/yes (extra charge)

Maximum No. of samples amplified in a single amplification event

384 samples (>384 samples with custom barcodes)

Read length/Percent bases >Q30

yes/up to 2 × 250 bp/up to 550 bp

Paired-end capability/Tag lengths/Spans

yes/up to 2 × 250 bp/up to 550 bp

Fragment/Tag lengths/Spans

yes/up to 2 × 250 bp/up to 550 bp

Mate pair/Tag lengths/Spans

yes/up to 2 × 250 bp/2–12 Kb

Single end/Tag lengths/Spans

yes/up to 1 × 300 bp/up to 350 bp

RNA sequencing/Tag lengths/Spans

yes/up to 2 × 250 bp/up to 500 bp

ChIP sequencing/Tag lengths/Spans

yes/up to 2 × 250 bp/up to 550 bp

Bisulfite sequencing/Tag lengths/Spans

yes/up to 2 × 250 bp/up to 550 bp

Maximum No. of reads or fragments sequenced per single-end run

up to 20 billion

Maximum No. of reads or fragments sequenced per paired-end run

up to 40 billion

Total No. of nucleotides (bases) sequenced per run

up to 6,000 Gb per run, 3,000 Gb per flow cell

Wet lab bench time for sequencing preparation

10 minutes

Sequencing run time

~13–44 hours

Total time for generating standard gDNA library

<3.5 hours (with Illumina DNA Prep)

• Paired end

<3.5 hours (with Illumina DNA Prep)

• Fragment

<7 hours (with AmpliSeq for Illumina); <6.5 hours (with Illumina DNA Prep with Enrichment)

• Paired end

• Fragment

• Mate pair

• Single end

<1 day (with TruSeq Small RNA)

• RNA sequencing

<9 hours

• ChIP sequencing

<1.5 days (with TruSeq ChIP)

• Bisulfite sequencing

Library preparation integrated in system as standard offering

no

Library preparation offered separately for additional charge

yes

Cost of sequencing reagents per run

$2,500–$17,300

Reagent tracking method

RFID

• Type of reagent information tracked

serial No., expiration date, lot and part Nos., No. of cycles

Shipping conditions for amplification/sequencing reagents

—/ice, dry ice, room temperature (variable based on product)

Storage conditions for amplification/sequencing reagents

—/cluster, SBS cartridges: -20°C; flow cell: 4°C; buffer cartridge: room temperature

Shelf life of amplification/sequencing reagents

—/guaranteed 6 months

System requires a control sample on sequencing run 

optional

• Company offers a sequencing control

yes (additional charge)

Sequencing system control software and devices to start run/for data analysis

NovaSeq 6000 Control Software/BaseSpace Sequence Hub

Complete walkaway automation for amplification, sequencing, and variant calling

no

Remote system monitoring

yes

Total time required for setup of amplification, sequencing, and variant calling steps

Maximum No. of libraries sequenced in a single run

384 samples (>384 samples with custom barcodes)

System includes secondary data-analysis software developed by company

yes (BaseSpace Sequence Hub)

System includes post-sequencing data-analysis software

no

Mutations detectable via data-analysis software

substitutions, indels, copy number changes

System can generate a variant report

no

Types of maintenance plans available/mean time between failures

parts only, bronze, silver, gold, dedicated on-site/—

No. of field application scientists and engineers based in U.S.

>500

• Weekly

• Monthly

none (maintenance or 4-lane post-run wash every 2 wks.)

• Pre-run

inspect and clean flow cell, flow-cell holder for debris; empty waste container

More products
in this guide

MiSeq i100 Plus
NextSeq 550Dx
NextSeq 1000; NextSeq 2000
NovaSeq 6000Dx
NovaSeq X; NovaSeq X Plus
Ion GeneStudio S5 System
Ion Torrent Genexus Integrated Sequencer; Ion Torrent Genexus Dx Integrated Sequencer