Indexed keywords
ARTICLE;
BAYES THEOREM;
DNA LIBRARY;
DNA POLYMORPHISM;
EXPRESSED SEQUENCE TAG;
GENE EXPRESSION;
GENE MUTATION;
GENE SEQUENCE;
HUMAN;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
SINGLE NUCLEOTIDE POLYMORPHISM;
STATISTICAL ANALYSIS;
BASE SEQUENCE;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 22;
COLONY-STIMULATING FACTORS;
EXPRESSED SEQUENCE TAGS;
GENE LIBRARY;
GENETIC DISEASES, INBORN;
GENETIC MARKERS;
GENOME, HUMAN;
HLA-A ANTIGENS;
HUMAN;
MODELS, GENETIC;
MODELS, STATISTICAL;
MOLECULAR SEQUENCE DATA;
POLYMORPHISM (GENETICS);
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
PROTEINS;
SEQUENCE ALIGNMENT;
SEQUENCE HOMOLOGY, NUCLEIC ACID;
SUPPORT, NON-U.S. GOV'T;
SUPPORT, U.S. GOV'T, NON-P.H.S.;
SUPPORT, U.S. GOV'T, P.H.S.;
1
0026053092
Low nucleotide diversity in man
Li, W. & Sadler, L.A. Low nucleotide diversity in man. Genetics 129, 513-523 (1991).
(1991)
Genetics
, vol.129
, pp. 513-523
Li, W.1
Sadler, L.A.2
2
0029741063
The future of genetic studies of complex human diseases
Risch, N. & Merikangas, K. The future of genetic studies of complex human diseases. Science 273, 1516-1517 (1996).
(1996)
Science
, vol.273
, pp. 1516-1517
Risch, N.1
Merikangas, K.2
3
0032533647
A 4-Mb high-density single nucleotide polymorphism-based map around human APOE
Lai, E., Riley, J., Purvis, I. & Roses, A. A 4-Mb high-density single nucleotide polymorphism-based map around human APOE. Genomics 54, 31-38 (1998).
(1998)
Genomics
, vol.54
, pp. 31-38
Lai, E.1
Riley, J.2
Purvis, I.3
Roses, A.4
4
17344364213
DNA sequence diversity in a 9.7 kb region of the human lipoprotein lipase gene
Nickerson, D.A. et al. DNA sequence diversity in a 9.7 kb region of the human lipoprotein lipase gene. Nature Genet. 19, 233-240 (1998).
(1998)
Nature Genet.
, vol.19
, pp. 233-240
Nickerson, D.A.1
5
0032544280
A closer look at SNPs suggests difficulties
Pennisi, E. A closer look at SNPs suggests difficulties. Science 281, 1787-1789 (1998).
(1998)
Science
, vol.281
, pp. 1787-1789
Pennisi, E.1
6
0031669184
Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms
Taillon-Miller, P., Gu, Z., Li, Q., Hillier, L & Kwok, P.Y. Overlapping genomic sequences: a treasure trove of single-nucleotide polymorphisms Genome Res. 8, 748-754 (1998).
(1998)
Genome Res.
, vol.8
, pp. 748-754
Taillon-Miller, P.1
Gu, Z.2
Li, Q.3
Hillier, L.4
Kwok, P.Y.5
7
0032524383
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
Wang, D.G. et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 280, 1077-1082 (1998).
(1998)
Science
, vol.280
, pp. 1077-1082
Wang, D.G.1
8
0032997217
The essence of SNPs
Brookes, A.J. The essence of SNPs. Gene 234, 177-186 (1999).
(1999)
Gene
, vol.234
, pp. 177-186
Brookes, A.J.1
9
0032991552
Characterization of single-nucleotide polymorphisms in coding regions of human genes
Cargill, M. et al. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nature Genet. 22, 231-238 (1999).
(1999)
Nature Genet.
, vol.22
, pp. 231-238
Cargill, M.1
10
0032990407
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
Halushka, M.K. et al. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nature Genet. 22, 239-246 (1999).
(1999)
Nature Genet.
, vol.22
, pp. 239-246
Halushka, M.K.1
11
0033560279
Consortium plans free SNP map of human genome
Masood, E. Consortium plans free SNP map of human genome. Nature 398, 545-546 (1999).
(1999)
Nature
, vol.398
, pp. 545-546
Masood, E.1
12
0031256078
Pieces of the puzzle: Expressed sequence tags and the catalog of human genes
Schuler, G. Pieces of the puzzle: expressed sequence tags and the catalog of human genes. J. Mol. Med. 75, 694-698 (1997).
(1997)
J. Mol. Med.
, vol.75
, pp. 694-698
Schuler, G.1
13
0033018816
Reliable identification of large numbers of candidate SNPs from public EST data
Buetow, K.H., Edmonson, M.N. & Cassidy, A.B. Reliable identification of large numbers of candidate SNPs from public EST data. Nature Genet. 21, 323-325 (1999).
(1999)
Nature Genet.
, vol.21
, pp. 323-325
Buetow, K.H.1
Edmonson, M.N.2
Cassidy, A.B.3
14
0033015046
Mining SNPs from EST databases
Picoult-Newberg, L. et al. Mining SNPs from EST databases. Genome Res. 9, 167-174 (1999).
(1999)
Genome Res.
, vol.9
, pp. 167-174
Picoult-Newberg, L.1
15
0032706623
A general approach to single nudeotide polymorphism discovery
Marth, G.T. et al. A general approach to single nudeotide polymorphism discovery. Nature Genet. 23, 452-456 (1999).
(1999)
Nature Genet.
, vol.23
, pp. 452-456
Marth, G.T.1
16
0031953260
The mutation rate and cancer
Jackson, A.L. & Loeb, L.A. The mutation rate and cancer. Genetics 148, 1483-1490 (1998).
(1998)
Genetics
, vol.148
, pp. 1483-1490
Jackson, A.L.1
Loeb, L.A.2
17
0028019887
Gene discovery in dbEST
Boguski, M.S., Tolstoshev, C.M. & Bassett, D.E.J. Gene discovery in dbEST. Science 265, 1993-1994 (1994).
(1994)
Science
, vol.265
, pp. 1993-1994
Boguski, M.S.1
Tolstoshev, C.M.2
Bassett, D.E.J.3
18
0001665613
Abnormal human haemoglobin. III. The chemical difference between normal and sickle cell haemoglobins
Ingram, V.M. Abnormal human haemoglobin. III. The chemical difference between normal and sickle cell haemoglobins. Biochim. Biophys. Acta 36, 402-411 (1959).
(1959)
Biochim. Biophys. Acta
, vol.36
, pp. 402-411
Ingram, V.M.1
19
34347168717
Hemoglobin tacoma - A β-chain variant associated with increased hb A2
Baur, E.W. & Motulsky, A.G. Hemoglobin tacoma - a β-chain variant associated with increased hb A2. Humangenetik 1, 621-634 (1965).
(1965)
Humangenetik
, vol.1
, pp. 621-634
Baur, E.W.1
Motulsky, A.G.2
20
0031955518
Base-calling of automated sequencer traces using phred. I. Accuracy assessment
Ewing, B., Hillier, L., Wendl, M.C. & Green, P. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res. 8, 175-185 (1998).
(1998)
Genome Res.
, vol.8
, pp. 175-185
Ewing, B.1
Hillier, L.2
Wendl, M.C.3
Green, P.4
21
0031978181
Base-calling of automated sequencer traces using phred. II. Error probabilities
Ewing, B. & Green, P. Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res. 8, 186-194 (1998).
(1998)
Genome Res.
, vol.8
, pp. 186-194
Ewing, B.1
Green, P.2
22
0024804855
A simple and rapid method for HLA-DQA1 genotyping by digestion of PCR-amplified DNA with allele specific restriction endonucleases
Maeda, M. et al. A simple and rapid method for HLA-DQA1 genotyping by digestion of PCR-amplified DNA with allele specific restriction endonucleases. Tissue Antigens 34, 290-298 (1989).
(1989)
Tissue Antigens
, vol.34
, pp. 290-298
Maeda, M.1