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

Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.

Genomics - 1 Apr 2010

Summerer Daniel, Schracke Nadine, Wu Haiguo, Cheng Yang, Bau Stephan, Stähler Cord F, Stähler Peer F, Beier Markus

Abstract excerpt

Sequence capture methods for targeted next generation sequencing promise to massively reduce cost of genomics projects compared to untargeted sequencing. However, evaluated capture methods specifically dedicated to biologically relevant genomic regions are rare. Whole exome capture has been shown to be a powerful tool to discover the genetic origin of disease and provides a reduction in target size and thus...

Read the complete abstract on PubMed

Topics

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

Share to Exons
Share to Genomics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Screening Assays

Share to Neoplasms

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

Share to Sequence Alignment

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 20138981
DOI: 10.1016/j.ygeno.2010.01.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.PMID 20138981Read ↗

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

Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.Semantic proximity Read ↗

High-performance single-chip exon capture allows accurate whole exome sequencing using the Illumina Genome Analyzer.Semantic proximity Read ↗

A programmable method for massively parallel targeted sequencing.Semantic proximity Read ↗

Multiplex amplification of large sets of human exons.Semantic proximity Read ↗

Single-Cell Genetic Analysis Using Automated Microfluidics to Resolve Somatic Mosaicism.Semantic proximity Read ↗

Simultaneous DNA, RNA, and Protein Analysis from Single Cells Using a High-Throughput Microfluidic Workflow for Resolution of Genotype-to-Phenotype Modalities.Semantic proximity Read ↗

Custom long non-coding RNA capture enhances detection sensitivity in different human sample typesSemantic proximity Read ↗

Rapid and highly-specific generation of targeted DNA sequencing libraries enabled by linking capture probes with universal primersSemantic proximity Read ↗

A Method for Extending Target Regions of Genomic Profiling by Combining a Custom Probe Pool with a Commercial Targeted Panel.Semantic proximity Read ↗

Comparison of commercially available target enrichment methods for next-generation sequencing.Semantic proximity Read ↗

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

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