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

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer

16 Dec 2016

Abstract excerpt

No abstract is available from the source.

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 Genetic factors in colorectal cancer
Share to Genomics and Rare Diseases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 27993330
DOI: 10.1016/j.jmoldx.2016.10.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in CancerPMID 27993330Read ↗

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendationsSemantic proximity Read ↗

Sequence Variant Descriptions: HGVS Nomenclature and Mutalyzer.Semantic proximity Read ↗

Sequence Variant Interpretation 2.0: Perspective on New Guidelines for Sequence Variant Classification.Semantic proximity Read ↗

ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencingSemantic proximity Read ↗

A survey assessing adoption of the ACMG-AMP guidelines for interpreting sequence variants and identification of areas for continued improvementSemantic proximity Read ↗

The current state of clinical interpretation of sequence variants.Semantic proximity Read ↗

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.Semantic proximity Read ↗

Many mutations in cancers.Semantic proximity Read ↗

HGVS Recommendations for the Description of Sequence Variants: 2016 Update.Semantic proximity Read ↗

Tutorial for variant interrogation in tumor samples.Semantic proximity Read ↗

Synonymous Variants: Necessary Nuance in Our Understanding of Cancer Drivers and Treatment Outcomes.Semantic proximity Read ↗

Human sequence variation and mutation databases.Semantic proximity Read ↗

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