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

Small insertions and deletions (INDELs) in human genomes.

Human molecular genetics - 15 Oct 2010

Mullaney Julienne M, Mills Ryan E, Pittard W Stephen, Devine Scott E

Abstract excerpt

In this review, we focus on progress that has been made with detecting small insertions and deletions (INDELs) in human genomes. Over the past decade, several million small INDELs have been discovered in human populations and personal genomes. The amount of genetic variation that is caused by these small INDELs is substantial. The number of INDELs in human genomes is second only to the number of single nucleotide...

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 Mutagenesis, Insertional

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Polymorphism, Single Nucleotide

Share to Sequence Deletion

Source

Open in PubMed Open full text

Identifiers

PMID: 20858594
DOI: 10.1093/hmg/ddq400
PMCID: PMC2953750

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Small insertions and deletions (INDELs) in human genomes.PMID 20858594Read ↗

Natural genetic variation caused by small insertions and deletions in the human genome.Semantic proximity Read ↗

An initial map of insertion and deletion (INDEL) variation in the human genome.Semantic proximity Read ↗

Characterization of frequencies and distribution of single nucleotide insertions/deletions in the human genome.Semantic proximity Read ↗

Small insertions are more deleterious than small deletions in human genomes.Semantic proximity Read ↗

Systematic analysis of microRNA targeting impacted by small insertions and deletions in human genome.Semantic proximity Read ↗

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes.Semantic proximity Read ↗

Characterization of missing human genome sequences and copy-number polymorphic insertions.Semantic proximity Read ↗

Genome-wide characterization of insertion and deletion variation in chicken using next generation sequencing.Semantic proximity Read ↗

Identification and analysis of short indels inducing exon extension/shrinkage events.Semantic proximity Read ↗

Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum.Semantic proximity Read ↗

Characteristics of de novo structural changes in the human genome.Semantic proximity Read ↗

The discovery of human genetic variations and their use as disease markers: past, present and future.Semantic proximity Read ↗

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