Evaluation of coverage variation of SNP chips for genome-wide association studies.
about
Chapter 11: Genome-wide association studiesHuman genetics and genomics a decade after the release of the draft sequence of the human genomeGenome-wide association studies and the clinic: a focus on breast cancerSystematic evaluation of apoptotic pathway gene polymorphisms and lung cancer riskPerformance of genotype imputation for rare variants identified in exons and flanking regions of genesThe role of genetics in the etiology of schizophreniaRare variants create synthetic genome-wide associationsFamily-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing dataSupplementing high-density SNP microarrays for additional coverage of disease-related genes: addiction as a paradigm.Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population.Identifying tagging SNPs for African specific genetic variation from the African Diaspora GenomeThe impact of phenocopy on the genetic analysis of complex traits.Evaluation of candidate genes in a genome-wide association study of childhood asthma in MexicansGenome-wide association study of relative telomere length.A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery.Inflammation-related genetic variations and survival in patients with advanced non-small cell lung cancer receiving first-line chemotherapyGenome-wide approaches to schizophrenia.Comprehensive evaluation of SNP identification with the Restriction Enzyme-based Reduced Representation Library (RRL) methodGenotype imputation for African Americans using data from HapMap phase II versus 1000 genomes projects.Clinical implications of shared genetics and pathogenesis in autoimmune diseases.CANDID: a flexible method for prioritizing candidate genes for complex human traits.Associations between gene polymorphisms in fatty acid metabolism pathway and preterm delivery in a US urban black population.Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism.Current status on genome-metabolome-wide associations: an opportunity in nutrition research.Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samplesExamining markers in 8q24 to explain differences in evidence for association with cleft lip with/without cleft palate between Asians and EuropeansThe limits of genome-wide methods for pharmacogenomic testing.Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans.Genetic bases of stuttering: the state of the art, 2011.Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases.Genetics and sports.Genome-wide association studies--a summary for the clinical gastroenterologist.Genetics of chronic obstructive pulmonary disease: a succinct review, future avenues and prospective clinical applications.Finding common susceptibility variants for complex disease: past, present and future.Search for cancer risk factors with microarray-based genome-wide association studies.The discovery of human genetic variations and their use as disease markers: past, present and future.The development of genome-wide association studies and their application to complex diseases, including lupus.Prioritising Causal Genes at Type 2 Diabetes Risk Loci.Coverage and efficiency in current SNP chips.
P2860
Q21145310-7CD8CFDE-F5BD-451C-9B63-3150BCBBFA4DQ21245451-68A1DD31-E068-4905-B4C9-EB541DB771FAQ22064616-227E2F6F-2476-42B6-880D-C7B516173175Q28391725-A62ECF28-63E7-4703-A608-BAB86D0B2242Q28744692-D27974E1-0BFF-4CA5-8494-199419636E4FQ28748800-A20C9D95-DBFA-4F46-B24E-5908F9EADE7DQ29614955-DC261621-FC8C-44E2-BB8B-D1BF0EE8F392Q30995743-24D8AB9B-7451-4E59-A260-1D695CD80B0DQ33432804-72C7C301-5B9A-4A4D-BEA2-31A18D08A0DCQ33575082-A670AE60-B92D-4F24-9129-501769AB326EQ33588298-720D84E1-2BB0-4D8D-887A-A4848264F13AQ33649844-6EC0D547-371C-4506-86A0-C765D531A1C1Q33665090-CA5B943C-5014-4421-A45B-BF3D46DE16F3Q33900326-30E18388-9A1B-49CB-81EA-8F2B1898EE35Q33915049-8BC150CE-6398-4871-B541-4BC51B5F60F7Q34042809-8E85F39D-D05F-42C0-87A3-4D3F76E7A98EQ34076429-2D5D875F-51B0-4D89-BF84-2851AE04AB81Q34138007-FD8A3CAC-5CA5-4CFC-B755-2EC066B4A7B4Q34160555-3283DBDE-A24B-47AB-A43C-A8E94D5E0049Q34285635-9186BE78-2328-4931-938E-5447684D5809Q34365119-02941FDB-8325-4ED4-841C-FDA9325BD719Q35571604-0FB43EFB-1C92-4818-863F-72BBCF0DAD2BQ35991776-BC9C7932-91C5-41AD-8398-35458E9EB5B2Q36171511-59A1B143-5616-4CE7-A16C-A7EE9C04E38AQ36502008-05532709-09BF-4FE6-881A-176FA1C9B3F9Q36512658-0582B456-E08B-485A-B67B-14CD4C78B218Q36737897-6A029216-58AA-458E-9484-8280A7B22ABEQ36848413-913C12A7-FF8C-4885-9AA3-0343D62F44F9Q36895545-55C65EB1-C1EA-40B7-8CCE-AFFFC8E970F2Q36966058-E20FFFF7-B287-4756-B8DA-A06C5D2A25ADQ37351462-B4EFFF9F-4E9A-4D8B-B30C-DFA13E00DE5BQ37390141-458EC243-E7DB-488E-96BD-BD1706E6D856Q37422991-47352096-12D5-45B2-8E95-302AB4162398Q37448915-02BC1431-3426-4BFC-AFA3-13112564F206Q37538006-D1F42DAD-EB78-459C-A511-5A5C99CBB46EQ37706517-D3BE1D63-9859-44D8-8857-9AE8913572A1Q37756529-89814C43-EAFF-4C49-A115-A5AC59842136Q38149849-52A38371-94F3-4227-8C66-921CFBB80DF8Q38652496-0579FFFF-0201-49FE-A6AB-CBFFC48D94C1Q42104486-3D78981E-5305-4DB0-9634-09D81DD4BF39
P2860
Evaluation of coverage variation of SNP chips for genome-wide association studies.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@en
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@nl
type
label
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@en
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@nl
prefLabel
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@en
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@nl
P2093
P356
P1476
Evaluation of coverage variation of SNP chips for genome-wide association studies.
@en
P2093
P2888
P304
P356
10.1038/SJ.EJHG.5202007
P577
2008-02-06T00:00:00Z