Clinical OMICs - Volume 2, Issue 11 - (Page 3)
Molecular Diagnostics in Personalized Medicine
NGS-enabled multiplexing
strategies may help drug
developers and clinicians move
beyond the "one biomarker/
one drug" approach to
Prevail
companion diagnostics.
GENOMICS AIDS GESTATION OF
PRENATAL MOLECULAR DIAGNOSTIC TESTS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
New approaches in genomic medicine advanced over the past several years
are helping future parents eliminate the risk of common inherited genetic
abnormalities.
Regular Features
CLINICAL GENOMICS UPDATE. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Molecularly Targeted Agents in Personalized Cancer Therapy and
Diagnostics: SHIVA trial raises key questions on the efficacy of certain cancer
treatments and reveals importance of genomic analysis for effective therapy.
with next-generation
sequencing in your
clinical laboratory
INNOVATOR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Arivale Brings Genomics to the People
Wellness startup intends to democratize personalized medicine.
SNAPSHOT. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Noninvasive Prenatal Screening-Making the Case for Responsible
Innovation in Genetic Testing: Growth of NIPS has launched a crusade of hope
for the future of prenatal care; however, what are the limits?
The Ion PGM Dx System
™
Delivering on our commitment to empower clinical laboratories to help improve patient
outcomes, the Ion PGM™ Dx System enables you to develop diagnostic tests using
next-generation sequencing. Validated using challenging germline variants, with library
kits based on proven Ion AmpliSeq™ technology, the system enables accurate and reliable
genetic analysis from more clinical samples, even with a limited amount of DNA. All with
a high-level of reproducible performance you can trust, and the rapid turnaround time
you need, to enable personalized care. Pursue. Pioneer. Prevail.
CASE STUDY. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Innovation in Molecular Diagnostics Changes the Game in Cancer
Screening: Development of a new noninvasive cancer detection technique
creates potential shift in patient willingness to undergo cancer screening.
Learn more at thermofisher.com/pgm-dx
For In Vitro Diagnostic Use. © 2015 Thermo Fisher Scientifi c Inc. All rights reserved. All trademarks are the property of Thermo Fisher
Scientifi c and its subsidiaries unless otherwise specifi ed. CO017601 0915
COMPANION DIAGNOSTICS FOR CANCER: Will NGS Play a Role?. . . 8
The rapid accumulation of new knowledge on tumor biology resulting
from next-gen sequencing is forcing stakeholders to continually
rethink companion diagnostics.
Cover and above (top): iStock/tarmofoto
Above (bottom): iStock/kirstypargeter
www.clinicalomics.com
NEWS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
NEW PRODUCTS. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
MEETING ROUNDUP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
November 2015 Clinical OMICs
3
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http://www.clinicalomics.com
Table of Contents for the Digital Edition of Clinical OMICs - Volume 2, Issue 11
Contents
Clinical OMICs - Volume 2, Issue 11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol3iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_vol2iss1
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue15
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue14
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue13
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue12
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue11
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue10
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue9
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue8
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue7
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue6
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue5
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue4
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue3
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue2
https://www.nxtbook.com/nxtbooks/gen/clinical_omics_issue1
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