X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (649) 649
Publication (142) 142
Book Review (67) 67
Book Chapter (21) 21
Conference Proceeding (8) 8
Dissertation (1) 1
Government Document (1) 1
Streaming Video (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (581) 581
humans (563) 563
hapmap project (423) 423
polymorphism, single nucleotide (306) 306
genetics & heredity (263) 263
genomics (213) 213
genotype (182) 182
genetics (170) 170
linkage disequilibrium (160) 160
hapmap (158) 158
haplotypes (155) 155
genomes (151) 151
female (150) 150
research (145) 145
genome, human (138) 138
male (132) 132
genetic aspects (127) 127
gene frequency (121) 121
genetic variation (117) 117
genome-wide association study (116) 116
genome-wide association (112) 112
single nucleotide polymorphisms (110) 110
analysis (109) 109
algorithms (106) 106
association (104) 104
international hapmap project (102) 102
population genetics (102) 102
article (101) 101
studies (96) 96
population (95) 95
human genome (94) 94
biotechnology & applied microbiology (93) 93
research article (93) 93
genetics, population (92) 92
polymorphism, single nucleotide - genetics (89) 89
genes (88) 88
genetic predisposition to disease (86) 86
biochemistry & molecular biology (85) 85
gene expression (83) 83
models, genetic (83) 83
single-nucleotide polymorphism (82) 82
polymorphism (79) 79
alleles (73) 73
disease (73) 73
software (72) 72
medicine (70) 70
middle aged (69) 69
genetic research (66) 66
adult (65) 65
multidisciplinary sciences (64) 64
case-control studies (63) 63
computational biology (62) 62
european continental ancestry group - genetics (62) 62
biology (61) 61
mathematical & computational biology (60) 60
cancer (59) 59
biochemical research methods (58) 58
computer simulation (57) 57
variants (57) 57
risk (56) 56
human genetics (55) 55
science (54) 54
asian continental ancestry group - genetics (52) 52
mutation (52) 52
databases, genetic (51) 51
dna (50) 50
chromosome mapping (49) 49
identification (47) 47
susceptibility (47) 47
methods (46) 46
phenotype (45) 45
risk factors (45) 45
genetic markers (44) 44
snp (44) 44
aged (43) 43
chromosomes (42) 42
bioinformatics (41) 41
gene (41) 41
genotype & phenotype (40) 40
expression (39) 39
polymorphisms (39) 39
single nucleotide polymorphism (39) 39
single-nucleotide polymorphisms (39) 39
usage (39) 39
data processing (38) 38
evolutionary biology (38) 38
loci (38) 38
quantitative trait loci (38) 38
deoxyribonucleic acid--dna (37) 37
genetic association studies (37) 37
genome-wide association studies (37) 37
genome (36) 36
inference (36) 36
molecular biology (36) 36
snps (36) 36
animals (35) 35
pharmacology & pharmacy (35) 35
african continental ancestry group - genetics (34) 34
medical research (34) 34
physiological aspects (34) 34
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Human Genetics, ISSN 1434-5161, 04/2018, Volume 63, Issue 4, pp. 533 - 536
Discoveries from the human genome, HapMap, and 1000 genome projects have collectively contributed toward the creation of a catalog of human genetic variations... 
DIVERSITY | KCNJ11 | GENE | ASSOCIATION | SEQUENCE | GENETICS & HEREDITY | Genetics, Population | HapMap Project | Humans | Arabs - genetics | United Arab Emirates | Genome, Human | Genomics - methods
Journal Article
Journal of the American Medical Informatics Association, ISSN 1067-5027, 03/2012, Volume 19, Issue 2, pp. 289 - 294
Journal Article
by Kaput, J and Cotton, R.G and Hardman, L and Watson, M and Aqeel, A.I. Al and Al-Aama, J.Y and Al-Mulla, F and Alonso, S and Aretz, S and Auerbach, A.D and Bapat, B and Bernstein, I.T and Bhak, J and Bleoo, S.L and Blocker, H and Brenner, S.E and Burn, J and Bustamante, M and Calzone, R and Cambon-Thomsen, A and Cargill, M and Carrera, P and Cavedon, L and Cho, Y.S and Chung, Y.J and Claustres, M and Cutting, G and Dalgleish, R and Dunnen, J.T. den and Diaz, C and Dobrowolski, S and Santos, M.R. dos and Ekong, R and Flanagan, S.B and Flicek, P and Furukawa, Y and Genuardi, M and Ghang, H and Golubenko, M.V and Greenblatt, M.S and Hamosh, A and Hancock, J.M and Hardison, R and Harrison, T.M and Hoffmann, R and Horaitis, R and Howard, H.J and Barash, C.I and Izagirre, N and Jung, J and Kojima, T and Laradi, S and Lee, Y.S and Lee, J.Y and Gil-da-Silva-Lopes, V.L and Macrae, F.A and Maglott, D and Marafie, M.J and Marsh, S.G and Matsubara, Y and Messiaen, L.M and Moslein, G and Netea, M.G and Norton, M.L and Oefner, P.J and Oetting, W.S and O'Leary, J.C and Ramirez, A.M. de and Paalman, M.H and Parboosingh, J and Patrinos, G.P and Perozzi, G and Phillips, I.R and Povey, S and Prasad, S and Qi, M and Quin, D.J and Ramesar, R.S and Richards, C.S and Savige, J and Scheible, D.G and Scott, R.J and Seminara, D and Shephard, E.A and Sijmons, R.H and Smith, T.D and Sobrido, M.J and Tanaka, T and Tavtigian, S.V and Taylor, G.R and Teague, J and Topel, T and Ullman-Cullere, M and Utsunomiya, J and Kranen, H.J. van and Vihinen, M and Webb, E and Weber, T.K and Yeager, M and Human Variome Project Planning and Contributors to the Human Variome Project Planning Meeting and on behalf of contributors to the Human Variome Project Planning Meeting
Human Mutation, ISSN 1059-7794, 2009, Volume 30, Issue 4, pp. 496 - 510
Journal Article
Frontiers in Genetics, ISSN 1664-8021, 2012, Volume 3, pp. 117 - 117
Genotype imputation is a vital tool in genome-wide association studies (GWAS) and meta-analyses of multiple GWAS results. Imputation enables researchers to... 
Genotype imputation | 1000 Genomes Project | HapMap Project | Latino | admixed populations | genotype imputation
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 11/2011, Volume 22, Issue 11, pp. 2129 - 2137
Journal Article
Journal Article
International Journal of Legal Medicine, ISSN 0937-9827, 9/2008, Volume 122, Issue 5, pp. 435 - 440
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 04/2013, Volume 41, Issue 7, pp. e90 - e90
We propose a novel approach to background correction for Infinium HumanMethylation data to account for technical variation in background fluorescence signal.... 
BACKGROUND CORRECTION | PATTERNS | MICROARRAY | CONVOLUTION MODEL | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA Methylation | HapMap Project | Oligonucleotide Array Sequence Analysis - methods | Humans | Fluorescent Dyes | Index Medicus | Methods Online
Journal Article