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

HORIBA

Yumizen C1200

Company

HORIBA

Name of instrument

Yumizen C1200

Contact

Susan Behnke  

Email

medical-marketing.us@horiba.com

City, State

Irvine, CA

Phone

888-903-5001  

Website

https://www.horiba.com/us/en/medical/

Type of instrument

chemistry

Operational type/Model type

continuous random access/floor standing

List price/First year sold in U.S.

$179, 800/2020

Targeted hospital bed size/Targeted test volume

< 300/daily: 9, 520; monthly: 17, 000; annual: 2 million

Company manufactures instrument

yes (manufactured by HORIBA ABX SAS; also sold by distribution partners)

Other models in this family of analyzers

Yumizen C1200 AL

No. of units in clinical use in U.S./Outside U.S. (countries)

Dimensions (H × W × D)/Instrument footprint

44 x 48 x 33.5 in./—

Weight empty/Weight fully loaded

992 lbs./—

No. of different measured assays onboard simultaneously

45 (45 can be run and calibrated at one time) 

No. of user-definable (open chemistry) channels

100 (100 can be active simultaneously)

Test throughput per hour/Assay run time

1, 200 (45 plus 3 ISE tests in throughput)/3–15 min.

No. of direct ion-selective electrode channels

3

Detection methods

photometry, potentiometry, enzyme immunoassay, immunoturbidimetry

• Ion-selective electrode

2.4 min./200 specimens per hr.

• Basic metabolic panel

12 min./60 specimens per hr.

• Complete metabolic panel

12 min./58 specimens per hr.

Typical time delay from ordering stat test until aspiration of sample

81 sec.

Fully automated microplate immunoassay system

Methodologies supported

Separation methodologies

Stat time until completion of a ß-hCG test

Stat time until completion of a cTn test

• Typical time delay from test order to aspiration of sample

Approximate No. of tests per reagent set/Reagent type

500–2, 200/self-contained multiuse, open reagent system

Reagents refrigerated onboard/Reagents ready to use

yes (2°–8°C)/variable; reagent specific

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/dependent on reagent

Design of sample-handling system

84 sample continuous loading ring, optional autoloading rack

Uses washable cuvettes/Uses disposable cuvettes

yes/no (can store up to 231 cuvettes)

Min.–max. sample volume that can be aspirated at one time 

1–25 µL

Min. reaction volume/Min. specimen volume/Min. dead volume

80 µL/—/200 µL for primary tube sampling

Dedicated pediatric sample cup

yes (dead volume: 50 µL)

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/yes

Pierces caps on primary tubes

no

Protects against probe collision

yes

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

detection for hemolysis, icterus, lipemia, clots

Dilutes patient samples onboard/Susceptibility to carryover

yes/—

Sample volume can be diluted to rerun out-of-linear-range high results

yes

Sample volume can be concentrated to rerun out-of-linear-range low results

Analyzer requires dedicated water supply

yes (average of 20 L/hr. consumption during operation)

Autocalibration/Multipoint calibration supported

yes (calibrants can be stored onboard [ISE])/yes (recommended avg. frequency: with each test kit)

Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays

daily/for QC failure/for QC failure/per test kit/—

Automatic programmable start/Automatic programmable shutdown

yes (40 min. start-up time)/yes

Supports multiple QC lot numbers per analyte

no

Waste management

direct to drain

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128, EAN)/—

Lab can control analyzer from remote computer

no

Instrument can diagnose its own malfunctions

yes (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

yes

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

onboard/CGM Labdaq

LIS interface provided/Bidirectional interface capability

no/yes (broadcast download and host query)

Modem servicing provided/Service engineer on-site response time

no/< 24 hrs.

Mean time between failures

122 days (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 10–15 min. (walkaway); weekly: 20–30 min.; monthly: < 60 min.

Maintenance records kept onboard for user/vendor

no/no

Maintenance training demonstration module onboard

no

Training included with purchase/Avg. time for basic user training

yes (1 training slot)/3 days (at vendor or customer site)

Advanced operator training/Extra charge for follow-up or advanced training

yes (at vendor site)/yes

Warranty provided/Cost of annual service contract (24 h/7 d)

yes (contract dependent)/—

Distinguishing features (supplied by company)

microvolume technology for improved cost efficiency; big lab automation in a small footprint; processes 1, 200 tests per hour with ion-selective electrodes; 100 programmable applications; optional autoloader

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