Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers-Reference-Cited by-同舟云学术

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Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers

Published:2011-07-05 Issue:S4 Volume:12 Page:
ISSN:1471-2105
Container-title:BMC Bioinformatics
language:en
Short-container-title:BMC Bioinformatics

Author:

Thomas Philippe E,Klinger Roman,Furlong Laura I,Hofmann-Apitius Martin,Friedrich Christoph M

Publisher

Springer Science and Business Media LLC

Subject

Applied Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Structural Biology

Link

http://link.springer.com/content/pdf/10.1186/1471-2105-12-S4-S4.pdf

Reference76 articles.

1. Collins FS, Brooks LD, Chakravarti A: A DNA polymorphism discovery resource for research on human genetic variation. Genome Research. 1998, 8 (12): 1229-1231.

2. Rösler A, Bailey L, Jones S, Briggs J, Cuss S, Horsey I, Kenrick M, Kingsmore S, Kent L, Pickering J, Knott T, Shipstone E, Scozzafava G: Rolling circle amplification for scoring single nucleotide polymorphisms. Nucleosides Nucleotides Nucleic Acids. 2001, 20 (4-7): 893-894. 10.1081/NCN-100002453.

3. Ke X, Taylor MS, Cardon LR: Singleton SNPs in the human genome and implications for genome-wide association studies. European Journal of Human Genetics. 2008, 16 (4): 506-515. 10.1038/sj.ejhg.5201987.

4. Ingram VM: A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin. Nature. 1956, 178 (4537): 792-794. 10.1038/178792a0.

5. Chang JC, Kan YW: beta 0 thalassemia, a nonsense mutation in man. Proceedings of the National Academy of Sciences of the United States of America. 1979, 76 (6): 2886-2889. 10.1073/pnas.76.6.2886.

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