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

Polymorphism discovery in high-throughput resequenced microarray-enriched human genomic loci.

Journal of biomolecular techniques : JBT - 1 Dec 2009

Antipova Alena A, Sokolsky Tanya D, Clouser Christopher R, Dimalanta Eileen T, Hendrickson Cynthia L, Kosnopo Cisilya, Lee Clarence C, Ranade Swati S, Zhang Lei, Blanchard Alan P, McKernan Kevin J

Abstract excerpt

Identifying genetic variants and mutations that underlie human diseases requires development of robust, cost-effective tools for routine resequencing of regions of interest in the human genome. Here, we demonstrate that coupling Applied Biosystems SOLiD system-sequencing platform with microarray...

Read the complete abstract on PubMed

Topics

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

Share to Oligonucleotide Array Sequence Analysis
Share to Base Sequence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to Heterozygote

Share to Homozygote

Share to Polymorphism, Genetic

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 19949697
PMCID: PMC2777346

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19949697-2026-09-02.2. 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

Polymorphism discovery in high-throughput resequenced microarray-enriched human genomic loci.PMID 19949697Read ↗

High-throughput, high-accuracy array-based resequencing.Semantic proximity Read ↗

New developments in high-throughput resequencing and variation detection using high density microarrays.Semantic proximity Read ↗

Microarray-based genomic selection for high-throughput resequencing.Semantic proximity Read ↗

Genotyping platforms for mass-throughput genotyping with SNPs, including human genome-wide scans.Semantic proximity Read ↗

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.Semantic proximity Read ↗

Applications of whole-genome high-density SNP genotyping.Semantic proximity Read ↗

A genome-wide scalable SNP genotyping assay using microarray technology.Semantic proximity Read ↗

High-throughput polymorphism screening and genotyping with high-density oligonucleotide arrays.Semantic proximity Read ↗

Whole human exome capture for high-throughput sequencing.Semantic proximity Read ↗

Flexible use of high-density oligonucleotide arrays for single-nucleotide polymorphism discovery and validation.Semantic proximity Read ↗

Direct selection of human genomic loci by microarray hybridization.Semantic proximity Read ↗

Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.Semantic proximity Read ↗

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