Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Geigl, JB; Speicher, MR.
Single-cell isolation from cell suspensions and whole genome amplification from single cells to provide templates for CGH analysis.
Nat Protoc. 2007; 2(12): 3173-3184. Doi: 10.1038/nprot.2007.476
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Führende Autor*innen der Med Uni Graz
Geigl Jochen Bernd
Co-Autor*innen der Med Uni Graz
Speicher Michael
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
A comprehensive genomic analysis of single cells is instrumental for numerous applications in tumor genetics, clinical diagnostics and forensic analyses. Here, we provide a protocol for single-cell isolation and whole genome amplification, which includes the following stages: preparation of single-cell suspensions from blood or bone marrow samples and cancer cell lines; their characterization on the basis of morphology, interphase fluorescent in situ hybridization pattern and antibody staining; isolation of single cells by either laser microdissection or micromanipulation; and unbiased amplification of single-cell genomes by either linker-adaptor PCR or GenomePlex library technology. This protocol provides a suitable template to screen for chromosomal copy number changes by conventional comparative genomic hybridization (CGH) or array CGH. Expected results include the generation of several micrograms of DNA from single cells, which can be used for CGH or other analyses, such as sequencing. Using linker-adaptor PCR or GenomePlex library technology, the protocol takes 72 or 30 h, respectively.
Find related publications in this database (using NLM MeSH Indexing)
Cell Line, Tumor -
Cell Separation - methods
Gene Library - methods
Genomics - methods
Humans - methods
In Situ Hybridization, Fluorescence - methods
Nucleic Acid Amplification Techniques - methods
Oligonucleotide Array Sequence Analysis - methods

© Med Uni Graz Impressum