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Literature DB >> 12644628

A haplotype map of the human genome.

Michael Olivier.

Abstract

Entities: Species

Mesh：

Substances：
Genetic Markers

Year: 2003 PMID： 12644628 DOI： 10.1152/physiolgenomics.00178.2002

Source DB: PubMed Journal: Physiol Genomics ISSN： 1094-8341 Impact factor: 3.107

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Cited

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14 in total

1. Big data challenges in bone research: genome-wide association studies and next-generation sequencing.

Authors: Nerea Alonso; Gavin Lucas; Pirro Hysi
Journal: Bonekey Rep Date: 2015-02-11

2. The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.

Authors: Lian Deng; Boon Peng Hoh; Dongsheng Lu; Ruiqing Fu; Maude E Phipps; Shilin Li; Ab Rajab Nur-Shafawati; Wan Isa Hatin; Endom Ismail; Siti Shuhada Mokhtar; Li Jin; Bin Alwi Zilfalil; Christian R Marshall; Stephen W Scherer; Fahd Al-Mulla; Shuhua Xu
Journal: Hum Genet Date: 2014-06-11 Impact factor: 4.132

3. Distribution and linkage disequilibrium analysis of polymorphisms of GH1 gene in different populations of pigs associated with body size.

Authors: Yunyun Cheng; Songcai Liu; Dan Su; Chao Lu; Xin Zhang; Qingyan Wu; Siming Li; Haoyu Fu; Hao Yu; Linlin Hao
Journal: J Genet Date: 2016-03 Impact factor: 1.166

4. Tumor somatic mutations also existing as germline polymorphisms may help to identify functional SNPs from genome-wide association studies.

Authors: Ivan P Gorlov; Xiangjun Xia; Spiridon Tsavachidis; Olga Y Gorlova; Christopher I Amos
Journal: Carcinogenesis Date: 2020-10-15 Impact factor: 4.944

5. Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.

Authors: H Mei; M L Cuccaro; E R Martin
Journal: Am J Hum Genet Date: 2007-10-23 Impact factor: 11.025

A haplotype map of the human genome.

1. Big data challenges in bone research: genome-wide association studies and next-generation sequencing.

2. The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.

3. Distribution and linkage disequilibrium analysis of polymorphisms of GH1 gene in different populations of pigs associated with body size.

4. Tumor somatic mutations also existing as germline polymorphisms may help to identify functional SNPs from genome-wide association studies.

5. Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.

6. Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.

7. Limitations of the human reference genome for personalized genomics.

8. Phenotype-genotype association grid: a convenient method for summarizing multiple association analyses.

9. My sister's keeper?: genomic research and the identifiability of siblings.

Review 10. A primer for disease gene prioritization using next-generation sequencing data.