Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides

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Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides. / Jensen, L J; Andersen, K V; Svendsen, A; Kretzschmar, T.

In: Nucleic Acids Research, Vol. 26, No. 3, 1998, p. 697-702.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jensen, LJ, Andersen, KV, Svendsen, A & Kretzschmar, T 1998, 'Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides', Nucleic Acids Research, vol. 26, no. 3, pp. 697-702.

APA

Jensen, L. J., Andersen, K. V., Svendsen, A., & Kretzschmar, T. (1998). Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides. Nucleic Acids Research, 26(3), 697-702.

Vancouver

Jensen LJ, Andersen KV, Svendsen A, Kretzschmar T. Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides. Nucleic Acids Research. 1998;26(3):697-702.

Author

Jensen, L J ; Andersen, K V ; Svendsen, A ; Kretzschmar, T. / Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides. In: Nucleic Acids Research. 1998 ; Vol. 26, No. 3. pp. 697-702.

Bibtex

@article{b453919dc7774e23adedc1992afd5794,
title = "Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides",
abstract = "Protein engineering by inserting stretches of random DNA sequences into target genes in combination with adequate screening or selection methods is a versatile technique to elucidate and improve protein functions. Established compounds for generating semi-random DNA sequences are spiked oligonucleotides which are synthesised by interspersing wild type (wt) nucleotides of the target sequence with certain amounts of other nucleotides. Directed spiking strategies reduce the complexity of a library to a manageable format compared with completely random libraries. Computational algorithms render feasible the calculation of appropriate nucleotide mixtures to encode specified amino acid subpopulations. The crucial element in the ranking of spiked codons generated during an iterative algorithm is the scoring function. In this report three scoring functions are analysed: the sum-of-square-differences function s, a modified cubic function c, and a scoring function m derived from maximum likelihood considerations. The impact of these scoring functions on calculated amino acid distributions is demonstrated by an example of mutagenising a domain surrounding the active site serine of subtilisin-like proteases. At default weight settings of one for each amino acid, the new scoring function m is superior to functions s and c in finding matches to a given amino acid population.",
author = "Jensen, {L J} and Andersen, {K V} and A Svendsen and T Kretzschmar",
year = "1998",
language = "English",
volume = "26",
pages = "697--702",
journal = "Nucleic Acids Research",
issn = "0305-1048",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Scoring functions for computational algorithms applicable to the design of spiked oligonucleotides

AU - Jensen, L J

AU - Andersen, K V

AU - Svendsen, A

AU - Kretzschmar, T

PY - 1998

Y1 - 1998

N2 - Protein engineering by inserting stretches of random DNA sequences into target genes in combination with adequate screening or selection methods is a versatile technique to elucidate and improve protein functions. Established compounds for generating semi-random DNA sequences are spiked oligonucleotides which are synthesised by interspersing wild type (wt) nucleotides of the target sequence with certain amounts of other nucleotides. Directed spiking strategies reduce the complexity of a library to a manageable format compared with completely random libraries. Computational algorithms render feasible the calculation of appropriate nucleotide mixtures to encode specified amino acid subpopulations. The crucial element in the ranking of spiked codons generated during an iterative algorithm is the scoring function. In this report three scoring functions are analysed: the sum-of-square-differences function s, a modified cubic function c, and a scoring function m derived from maximum likelihood considerations. The impact of these scoring functions on calculated amino acid distributions is demonstrated by an example of mutagenising a domain surrounding the active site serine of subtilisin-like proteases. At default weight settings of one for each amino acid, the new scoring function m is superior to functions s and c in finding matches to a given amino acid population.

AB - Protein engineering by inserting stretches of random DNA sequences into target genes in combination with adequate screening or selection methods is a versatile technique to elucidate and improve protein functions. Established compounds for generating semi-random DNA sequences are spiked oligonucleotides which are synthesised by interspersing wild type (wt) nucleotides of the target sequence with certain amounts of other nucleotides. Directed spiking strategies reduce the complexity of a library to a manageable format compared with completely random libraries. Computational algorithms render feasible the calculation of appropriate nucleotide mixtures to encode specified amino acid subpopulations. The crucial element in the ranking of spiked codons generated during an iterative algorithm is the scoring function. In this report three scoring functions are analysed: the sum-of-square-differences function s, a modified cubic function c, and a scoring function m derived from maximum likelihood considerations. The impact of these scoring functions on calculated amino acid distributions is demonstrated by an example of mutagenising a domain surrounding the active site serine of subtilisin-like proteases. At default weight settings of one for each amino acid, the new scoring function m is superior to functions s and c in finding matches to a given amino acid population.

M3 - Journal article

C2 - 9443959

VL - 26

SP - 697

EP - 702

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

IS - 3

ER -

ID: 40750041