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Article

Fishing for Function in the Human Gene Pool.

Trends in genetics : TIG - 1 Jul 2016

Barozzi Iros, Visel Axel, Dickel Diane E

Abstract excerpt

Identification and characterization of causal non-coding variants in human genomes is challenging and requires substantial experimental resources. A new study by Tehranchi et al. describes a cost-effective approach for accurate mapping of molecular quantitative trait loci (QTLs) from pooled samples, a powerful way to link disease-associated changes to molecular functions.

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Share to Chromosome Mapping
Share to Gene Pool
Share to Genetic Diseases, Inborn

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

Share to Genetic Variation

Share to Genome, Human

Share to Polymorphism, Single Nucleotide

Share to Quantitative Trait Loci

Share to Regulatory Sequences, Nucleic Acid

Source

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Identifiers

PMID: 27220646
DOI: 10.1016/j.tig.2016.05.002
PMCID: PMC4912909

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.

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