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

Human genome connectivity code links disease-associated SNPs, microRNAs and pyknons.

Cell cycle (Georgetown, Tex.) - 15 Mar 2009

Glinsky Gennadi V

Abstract excerpt

Discovery of pyknons, the most frequent, variable-length DNA sequence motifs in the human genomes, suggests extensive sequence-based connectivity between non-coding and protein-coding components of human genomes. Here we report identification of ubiquitous template design sequences (templum inten...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to MicroRNAs

Share to Molecular Sequence Data

Share to Polymorphism, Single Nucleotide

Share to Untranslated Regions

Source

Identifiers

PMID: 19229130
DOI: 10.4161/cc.8.6.7937

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19229130-2026-09-02.2. 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

Human genome connectivity code links disease-associated SNPs, microRNAs and pyknons.PMID 19229130Read ↗

A Mammalian Genomic Signature Shaped by Single Nucleotide Variants Regulates Transcriptome Integrity and DiversitySemantic proximity Read ↗

A mammalian genomic signature shaped by single nucleotide variants regulates transcriptome integrity and diversity.Semantic proximity Read ↗

G-quadruplex structural variations in human genome associated with single-nucleotide variations and their impact on gene activity.Semantic proximity Read ↗

Variation and selection at predicted G-quadruplexes across the human pangenomeSemantic proximity Read ↗

Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general populationSemantic proximity Read ↗

A Pāṇinian Grammar of the Human Genome: The Genomic Periodicity Index Encodes Functional Architecture and Evolutionary InnovationSemantic proximity Read ↗

Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs.Semantic proximity Read ↗

Profiling human pathogenic repeat expansion regions by synergistic and multi-level impacts on molecular connectionsSemantic proximity Read ↗

Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general population.Semantic proximity Read ↗

Integrative annotation of variants from 1092 humans: application to cancer genomics.Semantic proximity Read ↗

Characterizing regions in the human genome unmappable by next-generation-sequencing at the read length of 1000 bases.Semantic proximity Read ↗

Sequence-to-expression approach to identify etiological non-coding DNA variations in P53 and cMYC-driven diseasesSemantic proximity Read ↗

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