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

MAKING SENSE OF OUR VARIATION.

BioTechniques - 1 Nov 2015

Perkel Jeffrey

Abstract excerpt

Each human genome differs by millions of sequence variants, but which of these differences are important in human biology and disease? Jeffrey Perkel takes a look at the how scientists are identifying and cataloging important genetic variation.

Read the complete abstract on PubMed

Topics

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

Share to Genetic Variation
Share to Genome, Human
Share to Human Genome Project
Share to INDEL Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Nucleic Acid Conformation

Share to Polymorphism, Single Nucleotide

Share to RNA, Messenger

Share to United States

Source

Identifiers

PMID: 26554503
DOI: 10.2144/000114350

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MAKING SENSE OF OUR VARIATION.PMID 26554503Read ↗

Human genomics: A deep dive into genetic variation.Semantic proximity Read ↗

Researchers delve deeper into the human genome.Semantic proximity Read ↗

Genetics of complex diseases: knowing gene polymorphisms do matter.Semantic proximity Read ↗

Let's celebrate human genetic diversity.Semantic proximity Read ↗

Genomes in a bottle: creating standard reference materials for genomic variation - why, what and how?Semantic proximity Read ↗

Genetics. Toward a new vocabulary of human genetic variation.Semantic proximity Read ↗

Genetic variation: Diving deep into the genome.Semantic proximity Read ↗

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

Genetic variation in an individual human exome.Semantic proximity Read ↗

Mapping your profile. Scouting the human genome for clues to your health.Semantic proximity Read ↗

Finding the Rare Pathogenic Variants in a Human Genome.Semantic proximity Read ↗

Non-Coding Variation: The 2016 Annual Scientific Meeting of the Human Genome Variation Society.Semantic proximity Read ↗

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