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Literature DB >> 9872978

A DNA polymorphism discovery resource for research on human genetic variation.

F S Collins¹, L D Brooks, A Chakravarti.

Abstract

Entities: Species

Mesh：

Substances：
DNA

Year: 1998 PMID： 9872978 DOI： 10.1101/gr.8.12.1229

Source DB: PubMed Journal: Genome Res ISSN： 1088-9051 Impact factor: 9.043

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Cited

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205 in total

1. ALFRED: an allele frequency database for diverse populations and DNA polymorphisms.

Authors: K H Cheung; M V Osier; J R Kidd; A J Pakstis; P L Miller; K K Kidd
Journal: Nucleic Acids Res Date: 2000-01-01 Impact factor: 16.971

2. Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

Authors: D Fallin; A Cohen; L Essioux; I Chumakov; M Blumenfeld; D Cohen; N J Schork
Journal: Genome Res Date: 2001-01 Impact factor: 9.043

3. Fluorescence polarization in homogeneous nucleic acid analysis II: 5'-nuclease assay.

Authors: S Latif; I Bauer-Sardina; K Ranade; K J Livak; P Y Kwok
Journal: Genome Res Date: 2001-03 Impact factor: 9.043

4. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Authors: I N Bespalova; G Van Camp; S J Bom; D J Brown; K Cryns; A T DeWan; A E Erson; K Flothmann; H P Kunst; P Kurnool; T A Sivakumaran; C W Cremers; S M Leal; M Burmeister; M M Lesperance
Journal: Hum Mol Genet Date: 2001-10-15 Impact factor: 6.150

5. Pyrosequencing as a method for grouping of Listeria monocytogenes strains on the basis of single-nucleotide polymorphisms in the inlB gene.

Authors: H Unnerstad; H Ericsson; A Alderborn; W Tham; M L Danielsson-Tham; J G Mattsson
Journal: Appl Environ Microbiol Date: 2001-11 Impact factor: 4.792

6. A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.

Authors: D Gordon; S C Heath; X Liu; J Ott
Journal: Am J Hum Genet Date: 2001-07-05 Impact factor: 11.025

A DNA polymorphism discovery resource for research on human genetic variation.

1. ALFRED: an allele frequency database for diverse populations and DNA polymorphisms.

2. Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease.

3. Fluorescence polarization in homogeneous nucleic acid analysis II: 5'-nuclease assay.

4. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

5. Pyrosequencing as a method for grouping of Listeria monocytogenes strains on the basis of single-nucleotide polymorphisms in the inlB gene.

6. A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.

7. Trimming, weighting, and grouping SNPs in human case-control association studies.

8. High-throughput variation detection and genotyping using microarrays.

9. Molecular characterization of chicken syndecan-2 proteoglycan.

Review 10. Use of single nucleotide polymorphisms for gene discovery in hypertension.