Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS
Ehrich M, Böcker S, Boom D van den (2005)
Nucleic Acids Research 33(4): e38.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
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Autor*in
Ehrich, Mathias;
Böcker, Sebastian;
Boom, Dirk van den
Einrichtung
Abstract / Bemerkung
The completion of the Human Genome Project provides researchers with a reference sequence that covers about 99% of the gene-containing regions and is more than 99.9% accurate. Sequence drafts and completed sequences for several other species are also available to researchers worldwide. The ongoing effort to provide more and more genomic reference information now enables the detection of deviations from this `genetic blueprint'. Comparative sequencing projects will play a major role in elucidating the meaning of the genetic code and in establishing a correlation between genotype and phenotype. As part of this effort, a number of projects will focus on distinct functional aspects, like resequencing of exons or HLA determining regions. Typically these target regions are short in length and their analysis does not require long read length. To find an efficient solution for these applications, we developed a novel method that allows simultaneous analysis of multiple independent target regions (Multiplexed Comparative Sequence Analysis) by employing base-specific cleavage biochemistry and MALDI TOF-MS analysis.
Erscheinungsjahr
2005
Zeitschriftentitel
Nucleic Acids Research
Band
33
Ausgabe
4
Seite(n)
e38
ISSN
1362-4962
eISSN
1362-4962
Page URI
https://pub.uni-bielefeld.de/record/1773690
Zitieren
Ehrich M, Böcker S, Boom D van den. Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research. 2005;33(4):e38.
Ehrich, M., Böcker, S., & Boom, D. van den (2005). Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research, 33(4), e38. https://doi.org/10.1093/nar/gni038
Ehrich, Mathias, Böcker, Sebastian, and Boom, Dirk van den. 2005. “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”. Nucleic Acids Research 33 (4): e38.
Ehrich, M., Böcker, S., and Boom, D. van den (2005). Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research 33, e38.
Ehrich, M., Böcker, S., & Boom, D. van den, 2005. Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research, 33(4), p e38.
M. Ehrich, S. Böcker, and D. van den Boom, “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”, Nucleic Acids Research, vol. 33, 2005, pp. e38.
Ehrich, M., Böcker, S., Boom, D. van den: Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS. Nucleic Acids Research. 33, e38 (2005).
Ehrich, Mathias, Böcker, Sebastian, and Boom, Dirk van den. “Multiplexed discovery of sequence polymorphisms using base-specific cleavage and MALDI-TOF MS”. Nucleic Acids Research 33.4 (2005): e38.
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Hartmer R, Storm N, Boecker S, Rodi CP, Hillenkamp F, Jurinke C, van den Boom D., Nucleic Acids Res. 31(9), 2003
PMID: 12711692
SNP and mutation discovery using base-specific cleavage and MALDI-TOF mass spectrometry.
Bocker S., Bioinformatics 19 Suppl 1(), 2003
PMID: 12855436
Bocker S., Bioinformatics 19 Suppl 1(), 2003
PMID: 12855436
Chemiluminescent DNA sequencing with multiplex labeling.
Olesen CE, Martin CS, Bronstein I., BioTechniques 15(3), 1993
PMID: 8217162
Olesen CE, Martin CS, Bronstein I., BioTechniques 15(3), 1993
PMID: 8217162
Enzyme-linked fluorescent detection for automated multiplex DNA sequencing.
Cherry JL, Young H, Di Sera LJ, Ferguson FM, Kimball AW, Dunn DM, Gesteland RF, Weiss RB., Genomics 20(1), 1994
PMID: 8020958
Cherry JL, Young H, Di Sera LJ, Ferguson FM, Kimball AW, Dunn DM, Gesteland RF, Weiss RB., Genomics 20(1), 1994
PMID: 8020958
High-throughput MALDI-TOF discovery of genomic sequence polymorphisms.
Stanssens P, Zabeau M, Meersseman G, Remes G, Gansemans Y, Storm N, Hartmer R, Honisch C, Rodi CP, Bocker S, van den Boom D., Genome Res. 14(1), 2004
PMID: 14707174
Stanssens P, Zabeau M, Meersseman G, Remes G, Gansemans Y, Storm N, Hartmer R, Honisch C, Rodi CP, Bocker S, van den Boom D., Genome Res. 14(1), 2004
PMID: 14707174
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