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

Somatic microindels: analysis in mouse soma and comparison with the human germline.

Human mutation - 1 Jan 2007

Gonzalez Kelly D, Hill Kathleen A, Li Kai, Li Wenyan, Scaringe William A, Wang Ji-Cheng, Gu Dongqing, Sommer Steve S

Abstract excerpt

Microindels, defined as mutations that result in a colocalized microinsertion and microdeletion with a net gain or loss of between 1 and 50 nucleotides, may be an important contributor to cancer. We report the first comprehensive analysis of somatic microindels. Our large database of mutations in...

Read the complete abstract on PubMed

Topics

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

Share to Eukaryotic Cells
Share to Germ Cells
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lac Repressors

Share to Mutagenesis, Insertional

Share to Nucleic Acid Conformation

Share to Organ Specificity

Share to Sex Characteristics

Source

Identifiers

PMID: 16977595
DOI: 10.1002/humu.20416

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16977595-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Somatic microindels: analysis in mouse soma and comparison with the human germline.PMID 16977595Read ↗

Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity.Semantic proximity Read ↗

The rate and spectrum of new mutations in mice inferred by long-read sequencing.Semantic proximity Read ↗

Microdeletions and microinsertions causing human genetic disease: common mechanisms of mutagenesis and the role of local DNA sequence complexity.Semantic proximity Read ↗

Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity.Semantic proximity Read ↗

Sequence-based characterization of structural variation in the mouse genome.Semantic proximity Read ↗

Efficient and multiplexed somatic genome editing with Cas12a miceSemantic proximity Read ↗

The mouse pink-eyed unstable mutation: a DNA duplication revealed by genome scanning.Semantic proximity Read ↗

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.Semantic proximity Read ↗

Efficient analysis of mouse genome sequences reveal many nonsense variants.Semantic proximity Read ↗

The Complete Genome Sequences, Unique Mutational Spectra, and Developmental Potency of Adult Neurons Revealed by Cloning.Semantic proximity Read ↗

Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesisSemantic proximity Read ↗

Genome-Wide Characterization of Somatic Mutation Patterns in Cloned Dogs Reveals Implications for Neuronal Function, Tumorigenesis, and Aging.Semantic proximity Read ↗

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