UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.
Search Articles
Human heredity, ISSN 0001-5652, 1/2012, Volume 73, Issue 1, pp. 18 - 25
Original Paper | 1000 Genomes Project | Genome-wide association study | HapMap Project | Imputation performance | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Computational Biology - methods | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Reproducibility of Results | Humans | Genotype | Polymorphism, Single Nucleotide | Genotype & phenotype | Heredity | Genomics | Polymorphism | Index Medicus
Journal Article
International journal of immunogenetics, ISSN 1744-3121, 04/2019, Volume 46, Issue 2, pp. 49 - 58
1000 genomes project | HapMap | asthma | Estonian biobank | liver disease | single nucleotide polymorphism | Immunology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Liver diseases | Genomics | Genetic research | Single nucleotide polymorphisms | Comparative analysis | Chromosomes | Asthma | Gene frequency | Alleles | Population studies | Genomes | Single-nucleotide polymorphism | Statistics | Population genetics | Minority & ethnic groups | Morbidity | Index Medicus
Journal Article
Annual review of medicine, ISSN 0066-4219, 2/2012, Volume 63, Issue 1, pp. 35 - 61
simple nucleotide variation (SNV) | whole-genome sequencing (WGS) | exome sequencing | structural variation | personal genomics | Simple nucleotide variation (SNV) | Personal genomics | Whole-genome sequencing (WGS) | Exome sequencing | Structural variation | Genetic Privacy | HapMap Project | Humans | Genetic Diseases, Inborn - genetics | Genetic Diseases, Inborn - diagnosis | Human Genome Project | Genome, Human - genetics | Research | Nucleotide sequencing | Genetic variation | Genomics | Human genetics | DNA sequencing | Genomes | Biological variation | Genetic disorders | Medical diagnosis | Index Medicus
Journal Article
Pharmacogenomics, ISSN 1462-2416, 02/2010, Volume 11, Issue 2, pp. 249 - 256
Drug response | HapMap | SNP | Genetic variation | Lymphoblastoid cell lines | Pharmacogenomics | Life Sciences & Biomedicine | Pharmacology & Pharmacy | Science & Technology | Genetic Variation | Pharmacogenetics - trends | Base Sequence | Humans | Drug Therapy | Drug Discovery | Genome, Human - genetics | Drugs | Genetic markers | pharmacogenomics | Cytotoxicity | Data processing | Genetic diversity | Genomes | Gene expression | Waves
Journal Article
Journal of genetics, ISSN 0022-1333, 12/2015, Volume 94, Issue 4, pp. 731 - 740
Life Sciences | Life Sciences, general | minor allele frequency | Microbial Genetics and Genomics | heterozygous rate | genomewide association studies | Evolutionary Biology | transition | transversion | genotype discordance | Plant Genetics & Genomics | Animal Genetics and Genomics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Gene Frequency - genetics | HapMap Project | Chromosome Mapping - methods | Humans | Linkage Disequilibrium - genetics | Polymorphism, Single Nucleotide - genetics | Genotype | Genome, Human - genetics | Genetic research | Single nucleotide polymorphisms | Analysis | Genomics | Genotype & phenotype | Genetics | Genomes | Genetic diversity | Polymorphism | Index Medicus
Journal Article
6.
Full Text
Genotype imputation for Latinos using the HapMap and 1000 Genomes Project reference panels
Frontiers in genetics, ISSN 1664-8021, 2012, Volume 3, pp. 117 - 117
Journal Article
Nucleic acids research, ISSN 0305-1048, 04/2013, Volume 41, Issue 7, pp. e90 - e90
Journal Article
Community genetics, ISSN 1422-2795, 1/2007, Volume 10, Issue 3, pp. 186 - 198
Case Report | Community consultation | Community engagement | Informed consent | Public consultation | International HapMap Project | Genetic variation research | Public, Environmental & Occupational Health | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Variation | Genetics, Population | Informed Consent | Humans | Parents | Adult | Female | Male | Chromosome Mapping | International Cooperation | Child | Human Genome Project
Journal Article
Genome research, ISSN 1088-9051, 07/2012, Volume 22, Issue 7, pp. 1243 - 1254
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Species Specificity | HapMap Project | Humans | RNA, Messenger - genetics | Gene Expression Regulation | Selection, Genetic | Genotype | MicroRNAs - metabolism | Genetic Loci | Gene Regulatory Networks | RNA, Messenger - metabolism | Animals | Ethnic Groups - genetics | Genetics, Population - methods | Cell Line, Tumor | MicroRNAs - genetics | Mutation | Genome, Human | Genotyping Techniques - methods | High-Throughput Nucleotide Sequencing - methods | Human Genome Project | Leukocytes - metabolism | Evolution, Molecular | Leukocytes - cytology | MicroRNA | Research | Gene expression | Genetic regulation | Index Medicus
Journal Article
Genome research, ISSN 1088-9051, 09/2013, Volume 23, Issue 9, pp. 1514 - 1521
Journal Article
Genetic epidemiology, ISSN 0741-0395, 2008, Volume 32, Issue 2, pp. 98 - 107
tagging | HapMap | linkage disequilibrium | Tagging | Linkage disequilibrium | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Mathematical & Computational Biology | Haplotypes | Genetics, Population | Gene Frequency | Humans | Child, Preschool | European Continental Ancestry Group | Male | Chromosome Mapping | Genetic Markers | Linkage Disequilibrium | Genetic Variation | Attention Deficit Disorder with Hyperactivity - genetics | Internationality | Adolescent | Female | Polymorphism, Single Nucleotide | Israel | Child | Index Medicus
Journal Article