COMPREHENSIVE AND COMPLEMENTARY SEQUENCING
We provide access to a portfolio of comprehensive genomic profiling services for a variety of clinical sequencing needs.
Tempus xG (Powered by GeneDx)
88-gene and 52-gene germline panels
xG+ (extended hereditary cancers)
xG (common hereditary cancers)
Tumor/normal match DNA sequencing
Tumor/normal matched design provides accurate insight through true somatic identification with 27.7% fewer false positives than tumor-only analysis*.
Whole transcriptome RNA sequencing with validated fusion detection
RNA fusion analysis provides clinically-validated fusion detection and can provide more results than DNA-only sequencing.
Auto-conversion option to liquid biopsy
In the event of insufficient tumor tissue, you can choose to still receive a blood-based result, through a simple automatic conversion selection, providing genomic results without a delay.
Concurrent and longitudinal testing options
Simultaneous tissue and liquid biopsy testing can provide a comprehensive view of your patient and may offer insight into the evolution of cancer care throughout the course of disease.
Structured clinical data integration
In a retrospective study, at least one clinical option was reported for 96% of the cohort on the basis of Tempus NGS and matched clinical data.*
*Beaubier et al. Nature Biotechnology. 2019.
Our online Hub allows you secure, fast, reliable access to patient report status and results. View interactive and in-depth next-generation sequencing results in the context of a patient’s clinical history, filterable treatment applications and clinical trials, and PDFs of all Tempus reports.
You will also have access to our near real-time support tool that connects you with up-to-date treatment options and relevant insights derived from real-world clinical evidence across millions of de-identified patient records, our vast library of molecular profiling data, and our advanced analytics and machine-learning algorithms.
Download the Tempus mobile app.After processing your entire order, we produce an order summary highlighting all key findings from the xT and xF tests along with additional tests like Tumor Origin, HRD, and DPYD, including actionable treatments, microsatellite instability (MSI) status, and tumor mutational burden (TMB) that can be quickly translated into cancer patient care.
Our reports are also embedded with Tempus Insights, patient-specific insights derived from real-world evidence to empower physicians with the necessary data to improve patient care.
Get in touch to learn more.Tempus is the first genomic sequencing company to incorporate both Memorial Sloan Kettering Cancer Center’s OncoKB and NCCN Clinical Practice Guidelines (NCCN Guidelines®) into our smart clinical reports. MSK OncoKB & NCCN are two of the most robust oncology databases in the world. With the integration of these trusted sources, you can:
With a dedicated team of integration experts, we offer a fully interoperable solution for clinical ordering and returning results back into an institution’s health IT systems. We can transform our report into discrete genomic data that can be loaded directly into your system(s) in industry standard HL7 format. In addition, we collaborate with partners to offer a fully interoperable structured result file format which can be parsed and loaded into an institution’s data ecosystem to power their precision medicine program.
To ease the clinical ordering workflow, we support the automation of appropriate and secure data sharing to power your precision medicine program with Tempus clinical support and advanced analytics. If you have already ordered Tempus through paper or online methods, we can historically backfill prior results into your system(s).
We understand the power of analytics and the positive impact it has on clinical support.
Contact us today.The Tempus Sequencing Lab
We operate CAP-accredited, CLIA-certified robotic sequencing labs in Chicago, Atlanta, and Raleigh with automated bioinformatics and variant classification reporting. Sequencing is completed within 8-10 days on average of receiving patient samples.
Download our lab overviewAS PUBLISHED IN NATURE BIOTECHNOLOGY JOURNAL
“Extensive molecular profiling combined with clinical data identifies targeted therapies and clinical trials […] and paired tumor/normal plus transcriptome sequencing outperforms tumor-only DNA panel testing.”
Combined DNA and RNA sequencing using Tempus|xT increased the high level therapy matching rate to 43.4% of patients.
Follow-Up Testing Covered Under Tempus Financial Assistance*
Any US-based patient who receives Tempus testing may apply for our Financial Assistance Program. If approved, the program covers all medically necessary xT (solid), xF (liquid) and xG (hereditary) testing within 18 months of approval.
* Tempus testing is always conducted based on the medical judgement of an ordering physician.This is the future of healthcare.
648 gene panel + Whole transcriptome RNA sequencing with validated fusion detection
Enriched for clinically relevant genes and genes of emerging clinical relevance
Immunotherapy Metrics: MSI Status, Tumor Mutational Burden (TMB)
IHC Options: Mismatch Repair (MMR), PD-L1 (22C3, SP142, and 28-8 clones)
Available Add-on Tests: Tumor Origin (TO), Homologous Recombination Deficiency (HRD), DPYD
A
B
C
D
E
F
G
H
I
J
K
L
M
N
P
Q
R
S
T
U
V
W
X
Y
Z
105-gene DNA panel
Targeted panel designed to detect actionable oncologic targets in plasma.
Immunotherapy Metrics: MSI Status
A
B
C
D
E
F
G
H
I
J
K
M
N
P
R
S
T
U
V
Targeted Panels of 88 (xG+) & 52 (xG) genes
Providing risk-assessment for hereditary cancer syndromes for patients and their families.
A
B
C
D
E
F
G
H
K
L
M
N
P
R
S
T
V
W