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

National Genome Initiatives in Europe and the United Kingdom in the Era of Whole-Genome Sequencing: A Comprehensive Review

21 Mar 2022

Abstract excerpt

Identification of genomic variability in population plays an important role in the clinical diagnostics of human genetic diseases. Thanks to rapid technological development in the field of massive parallel sequencing technologies, also known as next-generation sequencing (NGS), complex genomic analyses are now easier and cheaper than ever before, which consequently leads to more effective utilization of these...

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35328109
DOI: 10.3390/genes13030556

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

National Genome Initiatives in Europe and the United Kingdom in the Era of Whole-Genome Sequencing: A Comprehensive ReviewPMID 35328109Read ↗

[Whole-genome sequencing and its application in the research and diagnoses of genetic diseases].Semantic proximity Read ↗

Sequencing and annotated analysis of an Estonian human genome.Semantic proximity Read ↗

Whole-genome sequencing of half-a-million UK Biobank participantsSemantic proximity Read ↗

Recommendations for whole genome sequencing in diagnostics for rare diseases.Semantic proximity Read ↗

Comparative Genomics in Homo sapiens.Semantic proximity Read ↗

Whole genome sequencing in clinical practice.Semantic proximity Read ↗

Whole genome sequence of a Turkish individual.Semantic proximity Read ↗

Whole genome sequencing.Semantic proximity Read ↗

A global reference for human genetic variation.Semantic proximity Read ↗

Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives.Semantic proximity Read ↗

Next-generation sequencing applied to rare diseases genomics.Semantic proximity Read ↗

A glimpse into past, present, and future DNA sequencing.Semantic proximity Read ↗

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