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

Sequencing genes in silico using single nucleotide polymorphisms.

BMC genetics - 30 Jan 2012

Zhang Xinyi Cindy, Zhang Bo, Li Shuying Sue, Huang Xin, Hansen John A, Zhao Lue Ping

Abstract excerpt

BACKGROUND: The advent of high throughput sequencing technology has enabled the 1000 Genomes Project Pilot 3 to generate complete sequence data for more than 906 genes and 8,140 exons representing 697 subjects. The 1000 Genomes database provides a critical opportunity for further interpreting disease associations with single nucleotide polymorphisms (SNPs) discovered from genetic association studies. Currently,...

Read the complete abstract on PubMed

Topics

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

Share to Computational Biology
Share to Computers
Share to Diabetes Mellitus, Type 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to KCNJ11 gene

Share to Polymorphism, Single Nucleotide

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 22289434
DOI: 10.1186/1471-2156-13-6
PMCID: PMC3283449

Genes

KCNJ11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sequencing genes in silico using single nucleotide polymorphisms.PMID 22289434Read ↗

The predicted impact of coding single nucleotide polymorphisms database.Semantic proximity Read ↗

On the analysis of sequence data: testing for disease susceptibility loci using patterns of linkage disequilibrium.Semantic proximity Read ↗

Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes.Semantic proximity Read ↗

The role of single nucleotide polymorphisms (SNPs) in understanding complex disorders and pharmacogenomics.Semantic proximity Read ↗

Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located?Semantic proximity Read ↗

Large-scale validation of single nucleotide polymorphisms in gene regions.Semantic proximity Read ↗

Genome bioinformatic analysis of nonsynonymous SNPs.Semantic proximity Read ↗

Predicting multiallelic genes using unphased and flanking single nucleotide polymorphisms.Semantic proximity Read ↗

High Quality Phasing Using Linked-Read Whole Genome Sequencing of Patient Cohorts Informs Genetic Understanding of Complex TraitsSemantic proximity Read ↗

Haplotype estimation using sequencing reads.Semantic proximity Read ↗

SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.Semantic proximity Read ↗

Sequence variation and the biological function of genes: methodological and biological considerations.Semantic proximity Read ↗

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