메뉴 건너뛰기




Volumn 8, Issue 7, 1998, Pages 748-754

Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms

Author keywords

[No Author keywords available]

Indexed keywords

NUCLEOTIDE;

EID: 0031669184     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.8.7.748     Document Type: Article
Times cited : (147)

References (13)
  • 2
    • 0027433148 scopus 로고
    • A new five-year plan for the U.S. Human Genome Program
    • Collins, F.S. and D. Galas. 1993. A new five-year plan for the U.S. Human Genome Program. Science 262: 43-46.
    • (1993) Science , vol.262 , pp. 43-46
    • Collins, F.S.1    Galas, D.2
  • 3
    • 0030688004 scopus 로고    scopus 로고
    • Variations on a theme: Cataloging human DNA sequence variation
    • Collins, F.S., M.S. Guyer, and A. Chakravarti. 1997. Variations on a theme: Cataloging human DNA sequence variation. Science 278: 1580-1581.
    • (1997) Science , vol.278 , pp. 1580-1581
    • Collins, F.S.1    Guyer, M.S.2    Chakravarti, A.3
  • 4
    • 0021943341 scopus 로고
    • An estimate of unique DNA sequence heterozygosity in the human genome
    • Cooper, D.N., B.A. Smith, H.J. Cooke, S. Niemann, and J. Schmidtke. 1985. An estimate of unique DNA sequence heterozygosity in the human genome. Hum. Genet. 69: 201-205.
    • (1985) Hum. Genet. , vol.69 , pp. 201-205
    • Cooper, D.N.1    Smith, B.A.2    Cooke, H.J.3    Niemann, S.4    Schmidtke, J.5
  • 5
    • 0031955518 scopus 로고    scopus 로고
    • Basecalling of automated sequencer traces using PHRED. I. Accuracy assessment
    • Ewing, B.C., L. Hillier, M.C. Wendl, and P. Green. 1998. Basecalling of automated sequencer traces using PHRED. I. Accuracy assessment. Genome Res. 8: 175-185.
    • (1998) Genome Res. , vol.8 , pp. 175-185
    • Ewing, B.C.1    Hillier, L.2    Wendl, M.C.3    Green, P.4
  • 6
    • 0026254627 scopus 로고
    • OSP: A computer program for choosing PCR and DNA sequencing primers
    • Hillier, L. and P. Green. 1991. OSP: A computer program for choosing PCR and DNA sequencing primers. PCR Methods Applic. 1: 124-128.
    • (1991) PCR Methods Applic. , vol.1 , pp. 124-128
    • Hillier, L.1    Green, P.2
  • 8
    • 0030861903 scopus 로고    scopus 로고
    • The use of a genetic map of biallelic markers in linkage studies
    • Kruglyak, L. 1997. The use of a genetic map of biallelic markers in linkage studies. Nature Genet. 17: 21-24.
    • (1997) Nature Genet. , vol.17 , pp. 21-24
    • Kruglyak, L.1
  • 9
    • 0028086580 scopus 로고
    • Comparative analysis of human DNA variations by fluorescence-based sequencing of PCR products
    • Kwok, P.-Y., C. Carlson, T. Yager, W. Ankener, and D.A. Nickerson. 1994. Comparative analysis of human DNA variations by fluorescence-based sequencing of PCR products. Genomics 23: 138-144.
    • (1994) Genomics , vol.23 , pp. 138-144
    • Kwok, P.-Y.1    Carlson, C.2    Yager, T.3    Ankener, W.4    Nickerson, D.A.5
  • 10
    • 0030021312 scopus 로고    scopus 로고
    • Increasing the information content of STS-based genome maps: Identifying polymorphisms in mapped STSs
    • Kwok, P.-Y., Q. Deng, H. Zakeri, and D.A. Nickerson. 1996. Increasing the information content of STS-based genome maps: Identifying polymorphisms in mapped STSs. Genomics 31: 123-126.
    • (1996) Genomics , vol.31 , pp. 123-126
    • Kwok, P.-Y.1    Deng, Q.2    Zakeri, H.3    Nickerson, D.A.4
  • 12
    • 0030756695 scopus 로고    scopus 로고
    • Snipping away at genome patenting
    • Marshall, E. 1997. Snipping away at genome patenting. Science 277: 1752-1753.
    • (1997) Science , vol.277 , pp. 1752-1753
    • Marshall, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.