Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Next-Generation, Genome Sequencing-Based Biomarkers: Concerns and Challenges for Medical Practice

1 Aug 2010

Abstract excerpt

Current efforts to complete the driver mutations catalogue for each common complex disease, and to understand biological and molecular networks provides an exciting field for novel biomarkers.However, the road to reaching medical applications is still long and many challenges must be overcome."

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cancer Genomics and Diagnostics
Share to Ferroptosis and cancer prognosis
Share to Genetic factors in colorectal cancer

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 20701445
DOI: 10.2217/bmm.10.70

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Next-Generation, Genome Sequencing-Based Biomarkers: Concerns and Challenges for Medical PracticePMID 20701445Read ↗

Next-generation sequencing applied to molecular diagnosticsSemantic proximity Read ↗

Next-generation sequencing approaches for genetic mapping of complex diseases.Semantic proximity Read ↗

Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencingSemantic proximity Read ↗

The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treated.Semantic proximity Read ↗

Regulatory perspectives on next-generation sequencing and complementary diagnostics in Japan.Semantic proximity Read ↗

Next generation sequencing in clinical diagnosisSemantic proximity Read ↗

Genetics, Biomarkers, Hereditary Cancer Syndrome Diagnosis, Heterogeneity and Treatment: A ReviewSemantic proximity Read ↗

First-line genome sequencing is here to stay, but how crucial is clinical phenotyping going to be?Semantic proximity Read ↗

Whole-genome sequencing and disease-gene detectionSemantic proximity Read ↗

Human Mutation special issue on innovations in genomic diagnostics.Semantic proximity Read ↗

Genome sequencing in the clinic: the past, present, and future of genomic medicineSemantic proximity Read ↗

[NEW ERA OF PERSONALIZED MEDICINE THROUGH NEXT－GENERATION SEQUENCING].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.