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On the spot: very local chromosomal rearrangements
Over the last decade, the detection of chromosomal abnormalities has shifted from conventional karyotyping under a light microscope to molecular detection using microarrays. The latter technology identified copy number variation as a major source of variation in the human genome; moreover, copy numb...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of 1000 Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505860/ https://www.ncbi.nlm.nih.gov/pubmed/23189093 http://dx.doi.org/10.3410/B4-22 |
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author | Helsmoortel, Céline Vandeweyer, Geert Kooy, R. Frank |
author_facet | Helsmoortel, Céline Vandeweyer, Geert Kooy, R. Frank |
author_sort | Helsmoortel, Céline |
collection | PubMed |
description | Over the last decade, the detection of chromosomal abnormalities has shifted from conventional karyotyping under a light microscope to molecular detection using microarrays. The latter technology identified copy number variation as a major source of variation in the human genome; moreover, copy number variants were found responsible for 10-20% of cases of intellectual disability. Recent technological advances in microarray technology have also enabled the detection of very small local chromosomal rearrangements, sometimes affecting the function of only a single gene. Here, we illustrate how high resolution microarray analysis has led to increased insights into the contribution of specific genes in disease. |
format | Online Article Text |
id | pubmed-3505860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Faculty of 1000 Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35058602012-11-27 On the spot: very local chromosomal rearrangements Helsmoortel, Céline Vandeweyer, Geert Kooy, R. Frank F1000 Biol Rep Review Article Over the last decade, the detection of chromosomal abnormalities has shifted from conventional karyotyping under a light microscope to molecular detection using microarrays. The latter technology identified copy number variation as a major source of variation in the human genome; moreover, copy number variants were found responsible for 10-20% of cases of intellectual disability. Recent technological advances in microarray technology have also enabled the detection of very small local chromosomal rearrangements, sometimes affecting the function of only a single gene. Here, we illustrate how high resolution microarray analysis has led to increased insights into the contribution of specific genes in disease. Faculty of 1000 Ltd 2012-11-01 /pmc/articles/PMC3505860/ /pubmed/23189093 http://dx.doi.org/10.3410/B4-22 Text en © 2012 Faculty of 1000 Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use this work for commercial purposes |
spellingShingle | Review Article Helsmoortel, Céline Vandeweyer, Geert Kooy, R. Frank On the spot: very local chromosomal rearrangements |
title | On the spot: very local chromosomal rearrangements |
title_full | On the spot: very local chromosomal rearrangements |
title_fullStr | On the spot: very local chromosomal rearrangements |
title_full_unstemmed | On the spot: very local chromosomal rearrangements |
title_short | On the spot: very local chromosomal rearrangements |
title_sort | on the spot: very local chromosomal rearrangements |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3505860/ https://www.ncbi.nlm.nih.gov/pubmed/23189093 http://dx.doi.org/10.3410/B4-22 |
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