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
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Thermo Fisher Scientific
| Company | Thermo Fisher Scientific |
|---|---|
| Name of system | Ion GeneStudio S5 System |
| City, State | Carlsbad, CA |
| Phone | 800-955-6288 |
| Website | |
| System application/FDA cleared or approved | research use/not required |
| Country where designed/Manufactured | U.S./Singapore |
| First year sold in U.S./First year installed in U.S. | 2018/2018 |
| System sold internationally | yes (worldwide) |
| Dimensions of sequencer (H × W × D)/Footprint of sequencer | 62.5 × 34.0 × 36.7 in./8.7 sq. ft. |
| Accessory equipment supplied with sequencer at no cost | — |
| Type of computer supplied with sequencer | operating computer |
| Analysis options provided with sequencer | onboard, cloud based, local server |
| Where library preparation is performed | accessory equipment |
| Bioinformatics tools provided with sequencer | onboard, cloud based, local server |
| Sequencer supplied with UPS (uninterruptible power supply) | no |
| Electrical connection required for sequencer | 100–240 VAC at 50/60 Hz, 6.5–14.5 A |
| List price of entire sequencer and necessary components | — |
| Purchase options | purchase, trade in, lease, finance |
| Warranties offered | first year included with purchase; extended warranty available |
| Training included/Total time for basic training per operator | yes/1 day |
| Training location/Follow-up training available | at vendor office or 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 | — |
| Paired-end capability/Tag lengths/Spans | — |
| Fragment/Tag lengths/Spans | yes/—/up to 600 bp |
| Mate pair/Tag lengths/Spans | — |
| Single end/Tag lengths/Spans | yes/—/up to 400 bp |
| RNA sequencing/Tag lengths/Spans | yes/—/up to 400 bp |
| ChIP sequencing/Tag lengths/Spans | — |
| Bisulfite sequencing/Tag lengths/Spans | yes/—/up to 400 bp |
| Maximum No. of reads or fragments sequenced per single-end run | 2–130 million |
| Maximum No. of reads or fragments sequenced per paired-end run | — |
| Total No. of nucleotides (bases) sequenced per run | 20–25 Gb (Ion 550); 10–15 Gb (Ion 540); 3–4 Gb (Ion 530); 0.6–1 Gb (Ion 520); 0.3–0.5 Gb (Ion 510 chip) |
| Wet lab bench time for sequencing preparation | <45 minutes |
| Sequencing run time | 2.5–4 hours |
| Total time for generating standard gDNA library | — |
| • Paired end | — |
| • Fragment | 4–6 hours |
| • Paired end | |
| • Fragment | |
| • Mate pair | — |
| • Single end | 5–7 hours |
| • RNA sequencing | <6 hours |
| • ChIP sequencing | — |
| • Bisulfite sequencing | 5.5 hours |
| Library preparation integrated in system as standard offering | yes (Ion Chef) |
| Library preparation offered separately for additional charge | yes (Ion AmpliSeq kit for Chef DL8) |
| Cost of sequencing reagents per run | — |
| Reagent tracking method | RFID |
| • Type of reagent information tracked | expiration date, lot and part Nos. |
| Shipping conditions for amplification/sequencing reagents | 20°C, 4°C, ambient (variable based on product)/20°C, 4°C, ambient (variable based on product) |
| Storage conditions for amplification/sequencing reagents | 20°C, 4°C, ambient (variable based on product)/20°C, 4°C, ambient (variable based on product) |
| Shelf life of amplification/sequencing reagents | 12–36 months from manufacture date (variable based on product)/12–36 months from manufacture date (variable based on product) |
| 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 | Torrent Suite/Ion Reporter |
| Complete walkaway automation for amplification, sequencing, and variant calling | no (walkaway automation for sequencing, variant calling) |
| Remote system monitoring | — |
| Total time required for setup of amplification, sequencing, and variant calling steps | <30 minutes |
| Maximum No. of libraries sequenced in a single run | 384 samples |
| System includes secondary data-analysis software developed by company | yes (Torrent Suite, Ion Reporter) |
| System includes post-sequencing data-analysis software | yes (Torrent Suite, Ion Reporter) |
| Mutations detectable via data-analysis software | substitutions, indels, copy number changes, complex biomarkers MSI, TMB, HRD |
| System can generate a variant report | yes |
| Types of maintenance plans available/mean time between failures | AB Assurance/— |
| No. of field application scientists and engineers based in U.S. | 450 |
| • Weekly | — |
| • Monthly | — |
| • Pre-run | — |
| Distinguishing features of NGS system (supplied by company)Note: a dash in lieu of an answer means company did not answer question or question is not applicable | pre-prepared library to variant report in <24 hours with 30 minutes of hands-on time; start with as little as 1 ng of input DNA; flexible sequencing depth and sample number throughput |