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

Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting.

BMC genomics - 15 Apr 2013

Teer Jamie K, Johnston Jennifer J, Anzick Sarah L, Pineda Marbin, Stone Gary, Meltzer Paul S, Mullikin James C, Biesecker Leslie G

Abstract excerpt

BACKGROUND: Targeted capture, combined with massively-parallel sequencing, is a powerful technique that allows investigation of specific portions of the genome for less cost than whole genome sequencing. Several methods have been developed, and improvements have resulted in commercial products targeting the human or mouse exonic regions (the exome). In some cases it is desirable to custom-target other regions of...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes
Share to Flow Cytometry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to High-Throughput Nucleotide Sequencing

Share to INDEL Mutation

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 23586822
DOI: 10.1186/1471-2164-14-253
PMCID: PMC3637801

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting.PMID 23586822Read ↗

Whole exome capture in solution with 3 Gbp of data.Semantic proximity Read ↗

Single Nucleotide Polymorphism (SNP) and Antibody-based Cell Sorting (SNACS): A tool for demultiplexing single-cell DNA sequencing dataSemantic proximity Read ↗

Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.Semantic proximity Read ↗

Phased Genome Sequencing Through Chromosome Sorting.Semantic proximity Read ↗

Isolation and sequencing of a single copy of an introgressed chromosome from a complex genome for gene and SNP identification.Semantic proximity Read ↗

Comparison of solution-based exome capture methods for next generation sequencing.Semantic proximity Read ↗

Efficient and cost effective population resequencing by pooling and in-solution hybridization.Semantic proximity Read ↗

Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat.Semantic proximity Read ↗

Gene-specific FACS sorting method for target selection in high-throughput amplicon sequencing.Semantic proximity Read ↗

Isolation and Sequencing of a Single Copy of an Introgressed Chromosome From a Complex Genome for Gene and SNP IdentificationSemantic proximity Read ↗

Completely phased genome sequencing through chromosome sorting.Semantic proximity Read ↗

Enrichment of sequencing targets from the human genome by solution hybridization.Semantic proximity Read ↗

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