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1. Full Text Performance of Genotype Imputations Using Data from the 1000 Genomes Project
by Yun Ju Sung and Lihua Wang and Tuomo Rankinen and Claude Bouchard and D.C. Rao
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
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2. Full Text Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations
by Reisberg, Sulev and Galwey, Nicholas and Avillach, Paul and Sahlqvist, Anna‐Stina and Kolberg, Liis and Mägi, Reedik and Esko, Tõnu and Vilo, Jaak and James, Glen
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
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3. Full Text Human Genome Sequencing in Health and Disease
by Gonzaga-Jauregui, Claudia and Lupski, James R and Gibbs, Richard A
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
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4. Impact of the 1000 Genomes Project on the next wave of pharmacogenomic discovery
by Zhang, Wei and Dolan, M. Eileen
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
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5. Full Text Comparing genetic variants detected in the 1000 genomes project with SNPs determined by the International HapMap Consortium
by ZHANG, WENQIAN and NG, HUI WEN and SHU, MAO and LUO, HENG and SU, ZHENQIANG and GE, WEIGONG and PERKINS, ROGER and TONG, WEIDA and HONG, HUIXIAO
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
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6. Full Text Genotype imputation for Latinos using the HapMap and 1000 Genomes Project reference panels
by Gao, Xiaoyi and Haritunians, Talin and Marjoram, Paul and Mckean-Cowdin, Roberta and Torres, Mina and Taylor, Kent D and Rotter, Jerome I and Gauderman, William J and Varma, Rohit
Frontiers in genetics, ISSN 1664-8021, 2012, Volume 3, pp. 117 - 117
Genotype imputation | 1000 Genomes Project | HapMap Project | Latino | admixed populations | genotype imputation
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7. Full Text Low-level processing of Illumina Infinium DNA Methylation BeadArrays
by Triche, Timothy J and Weisenberger, Daniel J and Van Den Berg, David and Laird, Peter W and Siegmund, Kimberly D
Nucleic acids research, ISSN 0305-1048, 04/2013, Volume 41, Issue 7, pp. e90 - e90
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | DNA Methylation | HapMap Project | Oligonucleotide Array Sequence Analysis - methods | Humans | Fluorescent Dyes | Index Medicus | Methods Online
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8. Full Text Community Engagement and Informed Consent in the International HapMap Project
by Charles Rotimi and Mark Leppert and Ichiro Matsuda and Changqing Zeng and Houcan Zhang and Clement Adebamowo and Ike Ajayi and Toyin Aniagwu and Missy Dixon and Yoshimitsu Fukushima and Darryl Macer and Patricia Marshall and Chibuzor Nkwodimmah and Andy Peiffer and Charmaine Royal and Eiko Suda and Hui Zhao and Vivian Ota Wang and Jean McEwen and Internatl HapMap Consortium and International HapMap Consortium
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
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9. Full Text Impact of microRNA regulation on variation in human gene expression
by Lu, Jian and Clark, Andrew G
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
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10. Full Text Estimating and interpreting FST: The impact of rare variants
by Bhatia, Gaurav and Patterson, Nick and Sankararaman, Sriram and Price, Alkes L
Genome research, ISSN 1088-9051, 09/2013, Volume 23, Issue 9, pp. 1514 - 1521
HapMap Project | Humans | Models, Genetic | Polymorphism, Single Nucleotide | Genome, Human | Population - genetics | Sequence Analysis, DNA - methods | Population genetics | Genetic polymorphisms | Research | Index Medicus | Method
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11. Full Text Population differences in the International Multi-Centre ADHD Gene Project
by Neale, B and Sham, P.C and Purcell, S and Banaschewski, T and Buitelaar, J.K and Franke, B and Sonuga-Barke, E.J.S and Ebstein, R.P and Eisenberg, J and Mulligan, A and Gill, M and Manor, I and Miranda, A and Mulas, F and Oades, R.D and Roeyers, H and Rothenberger, A and Sergeant, J.A and Steinhausen, H.C and Taylor, E and Thompson, M and Chen, W and Zhou, K and Asherson, P and Faraone, S.V
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
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