A periodic pattern of SNPs in the human genome

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A periodic pattern of SNPs in the human genome. / Madsen, Bo Eskerod; Villesen, Palle; Wiuf, Carsten.

In: Genome Research, Vol. 17, No. 10, 01.10.2007, p. 1414-1419.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Madsen, BE, Villesen, P & Wiuf, C 2007, 'A periodic pattern of SNPs in the human genome', Genome Research, vol. 17, no. 10, pp. 1414-1419. https://doi.org/10.1101/gr.6223207

APA

Madsen, B. E., Villesen, P., & Wiuf, C. (2007). A periodic pattern of SNPs in the human genome. Genome Research, 17(10), 1414-1419. https://doi.org/10.1101/gr.6223207

Vancouver

Madsen BE, Villesen P, Wiuf C. A periodic pattern of SNPs in the human genome. Genome Research. 2007 Oct 1;17(10):1414-1419. https://doi.org/10.1101/gr.6223207

Author

Madsen, Bo Eskerod ; Villesen, Palle ; Wiuf, Carsten. / A periodic pattern of SNPs in the human genome. In: Genome Research. 2007 ; Vol. 17, No. 10. pp. 1414-1419.

Bibtex

@article{69a8ebaf559a48ff9a5e3ef753006081,
title = "A periodic pattern of SNPs in the human genome",
abstract = "By surveying a filtered, high-quality set of SNPs in the human genome, we have found that SNPs positioned 1, 2, 4, 6, or 8 bp apart are more frequent than SNPs positioned 3, 5, 7, or 9 bp apart. The observed pattern is not restricted to genomic regions that are known to cause sequencing or alignment errors, for example, transposable elements (SINE, LINE, and LTR), tandem repeats, and large duplicated regions. However, we found that the pattern is almost entirely confined to what we define as {"}periodic DNA.{"} Periodic DNA is a genomic region with a high degree of periodicity in nucleotide usage. It turned out that periodic DNA is mainly small regions (average length 16.9 bp), widely distributed in the genome. Furthermore, periodic DNA has a 1.8 times higher SNP density than the rest of the genome and SNPs inside periodic DNA have a significantly higher genotyping error rate than SNPs outside periodic DNA. Our results suggest that not all SNPs in the human genome are created by independent single nucleotide mutations, and that care should be taken in analysis of SNPs from periodic DNA. The latter may have important consequences for SNP and association studies.",
author = "Madsen, {Bo Eskerod} and Palle Villesen and Carsten Wiuf",
year = "2007",
month = oct,
day = "1",
doi = "10.1101/gr.6223207",
language = "English",
volume = "17",
pages = "1414--1419",
journal = "Genome Research",
issn = "1088-9051",
publisher = "Cold Spring Harbor Laboratory Press",
number = "10",

}

RIS

TY - JOUR

T1 - A periodic pattern of SNPs in the human genome

AU - Madsen, Bo Eskerod

AU - Villesen, Palle

AU - Wiuf, Carsten

PY - 2007/10/1

Y1 - 2007/10/1

N2 - By surveying a filtered, high-quality set of SNPs in the human genome, we have found that SNPs positioned 1, 2, 4, 6, or 8 bp apart are more frequent than SNPs positioned 3, 5, 7, or 9 bp apart. The observed pattern is not restricted to genomic regions that are known to cause sequencing or alignment errors, for example, transposable elements (SINE, LINE, and LTR), tandem repeats, and large duplicated regions. However, we found that the pattern is almost entirely confined to what we define as "periodic DNA." Periodic DNA is a genomic region with a high degree of periodicity in nucleotide usage. It turned out that periodic DNA is mainly small regions (average length 16.9 bp), widely distributed in the genome. Furthermore, periodic DNA has a 1.8 times higher SNP density than the rest of the genome and SNPs inside periodic DNA have a significantly higher genotyping error rate than SNPs outside periodic DNA. Our results suggest that not all SNPs in the human genome are created by independent single nucleotide mutations, and that care should be taken in analysis of SNPs from periodic DNA. The latter may have important consequences for SNP and association studies.

AB - By surveying a filtered, high-quality set of SNPs in the human genome, we have found that SNPs positioned 1, 2, 4, 6, or 8 bp apart are more frequent than SNPs positioned 3, 5, 7, or 9 bp apart. The observed pattern is not restricted to genomic regions that are known to cause sequencing or alignment errors, for example, transposable elements (SINE, LINE, and LTR), tandem repeats, and large duplicated regions. However, we found that the pattern is almost entirely confined to what we define as "periodic DNA." Periodic DNA is a genomic region with a high degree of periodicity in nucleotide usage. It turned out that periodic DNA is mainly small regions (average length 16.9 bp), widely distributed in the genome. Furthermore, periodic DNA has a 1.8 times higher SNP density than the rest of the genome and SNPs inside periodic DNA have a significantly higher genotyping error rate than SNPs outside periodic DNA. Our results suggest that not all SNPs in the human genome are created by independent single nucleotide mutations, and that care should be taken in analysis of SNPs from periodic DNA. The latter may have important consequences for SNP and association studies.

UR - http://www.scopus.com/inward/record.url?scp=34948839041&partnerID=8YFLogxK

U2 - 10.1101/gr.6223207

DO - 10.1101/gr.6223207

M3 - Journal article

C2 - 17673700

AN - SCOPUS:34948839041

VL - 17

SP - 1414

EP - 1419

JO - Genome Research

JF - Genome Research

SN - 1088-9051

IS - 10

ER -

ID: 203904004