Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays

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Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays. / Petersen, J.; Poulsen, L.; Petronis, S.; Birgens, H.; Dufva, M.

I: Nucleic Acids Research, Bind 36, Nr. 2, 2008, s. e10-.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Petersen, J, Poulsen, L, Petronis, S, Birgens, H & Dufva, M 2008, 'Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays', Nucleic Acids Research, bind 36, nr. 2, s. e10-.

APA

Petersen, J., Poulsen, L., Petronis, S., Birgens, H., & Dufva, M. (2008). Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays. Nucleic Acids Research, 36(2), e10-.

Vancouver

Petersen J, Poulsen L, Petronis S, Birgens H, Dufva M. Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays. Nucleic Acids Research. 2008;36(2):e10-.

Author

Petersen, J. ; Poulsen, L. ; Petronis, S. ; Birgens, H. ; Dufva, M. / Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays. I: Nucleic Acids Research. 2008 ; Bind 36, Nr. 2. s. e10-.

Bibtex

@article{d821f860f76711ddbf70000ea68e967b,
title = "Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays",
abstract = "DNA microarrays are generally operated at a single condition, which severely limits the freedom of designing probes for allele-specific hybridization assays. Here, we demonstrate a fluidic device for multi-stringency posthybridization washing of microarrays on microscope slides. This device is called a multi-thermal array washer (MTAW), and it has eight individually controlled heating zones, each of which corresponds to the location of a subarray on a slide. Allele-specific oligonucleotide probes for nine mutations in the beta-globin gene were spotted in eight identical subarrays at positions corresponding to the temperature zones of the MTAW. After hybridization with amplified patient material, the slides were mounted in the MTAW, and each subarray was exposed to different temperatures ranging from 22 to 40 degrees C. When processed in the MTAW, probes selected without considering melting temperature resulted in improved genotyping compared with probes selected according to theoretical melting temperature and run under one condition. In conclusion, the MTAW is a versatile tool that can facilitate screening of a large number of probes for genotyping assays and can also enhance the performance of diagnostic arrays Udgivelsesdato: 2008/2",
author = "J. Petersen and L. Poulsen and S. Petronis and H. Birgens and M. Dufva",
note = "Times Cited: 0ArticleEnglishDufva, MTech Univ Denmark, Dept Micro & Nanotechnol, Microarray Grp, Bld 345 E, DK-2800 Lyngby, DenmarkCited References Count: 38260PGOXFORD UNIV PRESSGREAT CLARENDON ST, OXFORD OX2 6DP, ENGLANDOXFORD",
year = "2008",
language = "English",
volume = "36",
pages = "e10--",
journal = "Nucleic Acids Research",
issn = "0305-1048",
publisher = "Oxford University Press",
number = "2",

}

RIS

TY - JOUR

T1 - Use of a multi-thermal washer for DNA microarrays simplifies probe design and gives robust genotyping assays

AU - Petersen, J.

AU - Poulsen, L.

AU - Petronis, S.

AU - Birgens, H.

AU - Dufva, M.

N1 - Times Cited: 0ArticleEnglishDufva, MTech Univ Denmark, Dept Micro & Nanotechnol, Microarray Grp, Bld 345 E, DK-2800 Lyngby, DenmarkCited References Count: 38260PGOXFORD UNIV PRESSGREAT CLARENDON ST, OXFORD OX2 6DP, ENGLANDOXFORD

PY - 2008

Y1 - 2008

N2 - DNA microarrays are generally operated at a single condition, which severely limits the freedom of designing probes for allele-specific hybridization assays. Here, we demonstrate a fluidic device for multi-stringency posthybridization washing of microarrays on microscope slides. This device is called a multi-thermal array washer (MTAW), and it has eight individually controlled heating zones, each of which corresponds to the location of a subarray on a slide. Allele-specific oligonucleotide probes for nine mutations in the beta-globin gene were spotted in eight identical subarrays at positions corresponding to the temperature zones of the MTAW. After hybridization with amplified patient material, the slides were mounted in the MTAW, and each subarray was exposed to different temperatures ranging from 22 to 40 degrees C. When processed in the MTAW, probes selected without considering melting temperature resulted in improved genotyping compared with probes selected according to theoretical melting temperature and run under one condition. In conclusion, the MTAW is a versatile tool that can facilitate screening of a large number of probes for genotyping assays and can also enhance the performance of diagnostic arrays Udgivelsesdato: 2008/2

AB - DNA microarrays are generally operated at a single condition, which severely limits the freedom of designing probes for allele-specific hybridization assays. Here, we demonstrate a fluidic device for multi-stringency posthybridization washing of microarrays on microscope slides. This device is called a multi-thermal array washer (MTAW), and it has eight individually controlled heating zones, each of which corresponds to the location of a subarray on a slide. Allele-specific oligonucleotide probes for nine mutations in the beta-globin gene were spotted in eight identical subarrays at positions corresponding to the temperature zones of the MTAW. After hybridization with amplified patient material, the slides were mounted in the MTAW, and each subarray was exposed to different temperatures ranging from 22 to 40 degrees C. When processed in the MTAW, probes selected without considering melting temperature resulted in improved genotyping compared with probes selected according to theoretical melting temperature and run under one condition. In conclusion, the MTAW is a versatile tool that can facilitate screening of a large number of probes for genotyping assays and can also enhance the performance of diagnostic arrays Udgivelsesdato: 2008/2

M3 - Journal article

VL - 36

SP - e10-

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

IS - 2

ER -

ID: 10246835