Human molecular cytogenetics : from cells to nucleotides

Detalhes bibliográficos
Autor(a) principal: Riegel, Mariluce
Data de Publicação: 2014
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/116775
Resumo: The field of cytogenetics has focused on studying the number, structure, function and origin of chromosomal abnormalities and the evolution of chromosomes. The development of fluorescent molecules that either directly or via an intermediate molecule bind to DNA has led to the development of fluorescent in situ hybridization (FISH), a technology linking cytogenetics to molecular genetics. This technique has a wide range of applications that increased the dimension of chromosome analysis. The field of cytogenetics is particularly important for medical diagnostics and research as well as for gene ordering and mapping. Furthermore, the increased application of molecular biology techniques, such as array-based technologies, has led to improved resolution, extending the recognized range of microdeletion/microduplication syndromes and genomic disorders. In adopting these newly expanded methods, cytogeneticists have used a range of technologies to study the association between visible chromosome rearrangements and defects at the single nucleotide level. Overall, molecular cytogenetic techniques offer a remarkable number of potential applications, ranging from physical mapping to clinical and evolutionary studies, making a powerful and informative complement to other molecular and genomic approaches. This manuscript does not present a detailed history of the development of molecular cytogenetics; however, references to historical reviews and experiments have been provided whenever possible. Herein, the basic principles of molecular cytogenetics, the technologies used to identify chromosomal rearrangements and copy number changes, and the applications for cytogenetics in biomedical diagnosis and research are presented and discussed.
id UFRGS-2_95f7f92c7595ae0491842f1c7c99fb69
oai_identifier_str oai:www.lume.ufrgs.br:10183/116775
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Riegel, Mariluce2015-05-21T02:01:26Z20141415-4757http://hdl.handle.net/10183/116775000942504The field of cytogenetics has focused on studying the number, structure, function and origin of chromosomal abnormalities and the evolution of chromosomes. The development of fluorescent molecules that either directly or via an intermediate molecule bind to DNA has led to the development of fluorescent in situ hybridization (FISH), a technology linking cytogenetics to molecular genetics. This technique has a wide range of applications that increased the dimension of chromosome analysis. The field of cytogenetics is particularly important for medical diagnostics and research as well as for gene ordering and mapping. Furthermore, the increased application of molecular biology techniques, such as array-based technologies, has led to improved resolution, extending the recognized range of microdeletion/microduplication syndromes and genomic disorders. In adopting these newly expanded methods, cytogeneticists have used a range of technologies to study the association between visible chromosome rearrangements and defects at the single nucleotide level. Overall, molecular cytogenetic techniques offer a remarkable number of potential applications, ranging from physical mapping to clinical and evolutionary studies, making a powerful and informative complement to other molecular and genomic approaches. This manuscript does not present a detailed history of the development of molecular cytogenetics; however, references to historical reviews and experiments have been provided whenever possible. Herein, the basic principles of molecular cytogenetics, the technologies used to identify chromosomal rearrangements and copy number changes, and the applications for cytogenetics in biomedical diagnosis and research are presented and discussed.application/pdfengGenetics and molecular biology. Ribeirão Preto, SP. Vol. 37, no. 1, suppl. 1 (2014), p. 194-209.CitogenéticaGenética médicaAnálise citogenéticaMolecular cytogeneticsFISHArray-CGHCopy number variationGenomic disordersHuman molecular cytogenetics : from cells to nucleotidesinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT000942504.pdf.txt000942504.pdf.txtExtracted Texttext/plain81093http://www.lume.ufrgs.br/bitstream/10183/116775/2/000942504.pdf.txt0349b67e3e58e2b00581d166fb916a64MD52ORIGINAL000942504.pdf000942504.pdfTexto completo (inglês)application/pdf2608377http://www.lume.ufrgs.br/bitstream/10183/116775/1/000942504.pdfc2ca9b0d2495a51a106f0b84232ded22MD51THUMBNAIL000942504.pdf.jpg000942504.pdf.jpgGenerated Thumbnailimage/jpeg1809http://www.lume.ufrgs.br/bitstream/10183/116775/3/000942504.pdf.jpg3a7ee4213839888c38e5182205cc1ff3MD5310183/1167752024-01-06 04:36:06.952134oai:www.lume.ufrgs.br:10183/116775Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-01-06T06:36:06Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Human molecular cytogenetics : from cells to nucleotides
title Human molecular cytogenetics : from cells to nucleotides
spellingShingle Human molecular cytogenetics : from cells to nucleotides
Riegel, Mariluce
Citogenética
Genética médica
Análise citogenética
Molecular cytogenetics
FISH
Array-CGH
Copy number variation
Genomic disorders
title_short Human molecular cytogenetics : from cells to nucleotides
title_full Human molecular cytogenetics : from cells to nucleotides
title_fullStr Human molecular cytogenetics : from cells to nucleotides
title_full_unstemmed Human molecular cytogenetics : from cells to nucleotides
title_sort Human molecular cytogenetics : from cells to nucleotides
author Riegel, Mariluce
author_facet Riegel, Mariluce
author_role author
dc.contributor.author.fl_str_mv Riegel, Mariluce
dc.subject.por.fl_str_mv Citogenética
Genética médica
Análise citogenética
topic Citogenética
Genética médica
Análise citogenética
Molecular cytogenetics
FISH
Array-CGH
Copy number variation
Genomic disorders
dc.subject.eng.fl_str_mv Molecular cytogenetics
FISH
Array-CGH
Copy number variation
Genomic disorders
description The field of cytogenetics has focused on studying the number, structure, function and origin of chromosomal abnormalities and the evolution of chromosomes. The development of fluorescent molecules that either directly or via an intermediate molecule bind to DNA has led to the development of fluorescent in situ hybridization (FISH), a technology linking cytogenetics to molecular genetics. This technique has a wide range of applications that increased the dimension of chromosome analysis. The field of cytogenetics is particularly important for medical diagnostics and research as well as for gene ordering and mapping. Furthermore, the increased application of molecular biology techniques, such as array-based technologies, has led to improved resolution, extending the recognized range of microdeletion/microduplication syndromes and genomic disorders. In adopting these newly expanded methods, cytogeneticists have used a range of technologies to study the association between visible chromosome rearrangements and defects at the single nucleotide level. Overall, molecular cytogenetic techniques offer a remarkable number of potential applications, ranging from physical mapping to clinical and evolutionary studies, making a powerful and informative complement to other molecular and genomic approaches. This manuscript does not present a detailed history of the development of molecular cytogenetics; however, references to historical reviews and experiments have been provided whenever possible. Herein, the basic principles of molecular cytogenetics, the technologies used to identify chromosomal rearrangements and copy number changes, and the applications for cytogenetics in biomedical diagnosis and research are presented and discussed.
publishDate 2014
dc.date.issued.fl_str_mv 2014
dc.date.accessioned.fl_str_mv 2015-05-21T02:01:26Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/other
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/116775
dc.identifier.issn.pt_BR.fl_str_mv 1415-4757
dc.identifier.nrb.pt_BR.fl_str_mv 000942504
identifier_str_mv 1415-4757
000942504
url http://hdl.handle.net/10183/116775
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Genetics and molecular biology. Ribeirão Preto, SP. Vol. 37, no. 1, suppl. 1 (2014), p. 194-209.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/116775/2/000942504.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/116775/1/000942504.pdf
http://www.lume.ufrgs.br/bitstream/10183/116775/3/000942504.pdf.jpg
bitstream.checksum.fl_str_mv 0349b67e3e58e2b00581d166fb916a64
c2ca9b0d2495a51a106f0b84232ded22
3a7ee4213839888c38e5182205cc1ff3
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1801224871440547840