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

Sysmex Corp.

pocH-100i

Company

Sysmex Corp.

Name of analyzer

pocH-100i

Contact

Madelaine Dintelman  

Email

[email protected]

City, State

Lincolnshire, IL

Phone

888-879-7639

Website

https://www.sysmex.com

Analyzer application

diagnostic use

Dimensions of analyzer (H × W ×

10.1 × 7.3 × 13.8 in./—

Country where analyzer was

Japan/Japan

First year analyzer was sold in U.S./Approximate No. of units installed in U.S.*

2004/>2, 000

First year analyzer sold outside

2003/>5, 000

Foreign locations where company

Human languages (other than

Analyzer list price

$21, 003.84 (slide maker stainer sold separately)

• Analyzer acquisition options

purchase, trade in, lease, cost per reportable contract

Training included with purchase/Total time for basic training per operator

<2 min. daily; <2 min. weekly; <2 min. monthly

• Follow-up training available

yes (no extra charge)

Parameters that analyzer tests and reports

%&# lymphocytes, %&# neutrophils, Hb, Hct, MCHC, MCV, PLT, RBC, WBC

Types of testing FDA cleared or approved for analyzer

Types of body fluids FDA cleared or approved for analysis on analyzer

Analytical measurement range for body fluid

Precision for body fluid

Accuracy for body fluid

Automated differential performed for body fluids

Tests available for research use only

Differential methods used

direct current

Analytical measurement range: • WBC count/RBC count

WBC: 1.0–99.9 × 103/μL/RBC: 0.3–7.0 × 106/μL

Precision: • WBC count/RBC count

WBC: ≤3.5%/RBC: ≤2.0%

Accuracy: • WBC count/RBC count

Interfering substances: • WBC/RBC

lyse-resistant RBCs, cold agglutinins, cryoglobulins, platelet aggregation, NRBCs/cold agglutinins, severe microcytosis, fragmented RBCs

• Hemoglobin/Platelets

severe lipemia, abnormal protein, leukocytosis (>100, 000/μL)/platelet aggregation, giant platelets, microcytic RBCs, fragmented RBCs

• Hematocrit/Reticulocytes

cold agglutinins, severe microcytosis, fragmented RBCs/—

• Automated differential

Throughput: max. CBCs per hour/Max. CBCs with differentials per hour

30/30

• Max. No. of slides processed per hour if stainer included

FDA-cleared or -approved sample container types (besides potassium EDTA)

none

Min. specimen volume open mode/Closed mode/Microsample capability

15 µL/15 µL/yes

Types of patient data archived/Max. No. of archived patient data accessible when analyzer online

flags, histograms/100 samples

Analyzer performs delta checks

yes

Parameters for which flags may appear

flagging system suggests sample error for WBC, RBC, platelet parameters

Analyzer recognizes and holds test results

no

Scattergram display uses cell-specific color

no

Histogram display uses color with thresholds

yes

LIS interface formats supported

ASTM 1381, ASTM 1394-97, RS-232C

• Middleware interface

yes (can use company’s middleware or Data Innovations)

• Information transferred to LIS via middleware or LIS interface

numeric results, flagged results, histograms, scatterplots, patient demographics, patient orders, host query for patient demographics and orders

Analyzer transmits LOINC codes for results to LIS or middleware

no (provides list of machine codes for each test and corresponding LOINC code)

Lab automation system or workcells to which analyzer has a direct interface

none

Barcode symbologies read on specimen tube

Code 39, Code 128, ASTM, ITF, NW-7, JAN-8, JAN-13

• Analyzer allows barcode placement per CLSI standard Auto02-A2

no

No. of onboard reagents required for standard specimen analysis

2

• Reagents ready to use/Reagent tracking method

yes/barcode reader

Onboard diagnostics for troubleshooting

yes

• Manufacturer can perform diagnostics via remote access

yes

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

one-year warranty/—

Notes

†also marketed by McKesson, Henry Schein

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