Webinars and Sponsored Roundtables — Register Now
Wednesday, September 30, 2026. 1 PM-1:30 PM ET
Roundtable presenters John Longshore, PhD, Head of Scientific Affairs, Global Oncology Diagnostics, AstraZeneca, and Flora Berisha, MS, Executive Director, Global Head of Diagnostic Partnering and Development, Johnson & Johnson Innovative Medicine, and Mark D. Ewalt, MD, Associate Medical Director for Laboratory Operations, Diagnostic Molecular Pathology, Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, and Isabel Preeshagul, DO, MBS, Thoracic Medical Oncologist, Memorial Sloan Kettering Cancer Center
CAP TODAY does not endorse any of the products or services named within. The roundtable is made possible by a special educational grant from Pillar Biosciences.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Thursday, October 1, 2026 1 PM-2 PM ET
This presentation will explore the value of in-house CGP, offer insights into the benefits and drawbacks of incorporation, and provide information about important practical factors when considering in-house implementation of CGP.
Webinar presenter Allison M. Cushman-Vokoun, MD, PhD, FCAP, Medical Director, Molecular Diagnostics and Personalized Medicine Laboratory, Director, Division of Diagnostic Molecular Pathology and Human Genetics, Henry F. Krous Professor of Pathology, University of Nebraska Medical Center
CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Illumina.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Tuesday, October 20, 2026 11 AM-12 PM ET
Hear experts review the biological and clinical significance of the HER2 expression continuum in breast tissue, providing a clearer understanding of how these variations might impact diagnosis, and discuss the emerging importance of documenting HER2-low and HER2-ultralow categories using a validated IHC assay.
Webinar presenters Keith Wharton, MD, PhD, Global Medical Affairs Leader–Pathology, Roche Diagnostics Solutions, and Hannah Y. Wen, MD, PhD, Director, Breast Pathology Fellowship, Associate Team Leader, Breast Pathology Team, Attending Pathologist, Memorial Sloan Kettering Cancer Center
CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Roche.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Tuesday, November 3, 2026 1 PM-2 PM ET
Hear an expert discuss the challenges of detecting NRG1 fusions and how RNA-based testing can support more comprehensive fusion identification in clinical practice.
Webinar presenter Benjamin Weinberg, MD, Associate Professor of Medicine and Attending Physician
specializing in gastrointestinal medical oncology
CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Diaceutics.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Interactive Product Guides
Product Spotlight
Thermo Fisher Scientific
Ion GeneStudio S5 System
| 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 | Torrent Suite (optional: Ion Reporter, Oncomine Reporter) |
| 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 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 | up to 600 bp/— |
| 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 |
| • Mate pair | — |
| • Single end | 5–7 hours |
| • RNA sequencing | <6 hours |
| • Bisulfite sequencing | 5.5 hours |
| • Hands-on time for paired end | — |
| • Hands-on time for fragment | 1 hour |
| • Hands-on time for mate pair | <1 hour |
| • Hands-on time for single end | 15 minutes |
| • Hands-on time for RNA sequencing | 1 hour (with Ion AmpliSeq Transcriptome) |
| • Hands-on time for ChIP sequencing | — |
| • Hands-on time for bisulfite sequencing | 30 minutes |
| Library preparation integrated in system as standard offering | no (performed on Ion Chef) |
| 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 |
| 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 maintenance required | — |
| • Monthly maintenance required | — |
| • Pre-run maintenance required | — |
| Distinguishing features of NGS system (supplied by company) | scalable, flexible, end-to-end NGS solution from library to report with turnaround time of <24 hours and <45 minutes of hands-on time; start with as little as 1 ng of input DNA or RNA; flexible sequencing depth and sample number throughput |