Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms-Reference-Cited by-同舟云学术

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Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms

Published:2015-03-23 Issue:5 Volume:12 Page:458-464
ISSN:1548-7091
Container-title:Nature Methods
language:en
Short-container-title:Nat Methods

Author:

del Rosario Ricardo Cruz-Herrera,Poschmann Jeremie,Rouam Sigrid Laure,Png Eileen,Khor Chiea Chuen,Hibberd Martin Lloyd,Prabhakar Shyam

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Biochemistry,Biotechnology

Link

http://www.nature.com/articles/nmeth.3326.pdf

Reference54 articles.

1. Boyle, A.P. et al. Annotation of functional variation in personal genomes using RegulomeDB. Genome Res. 22, 1790–1797 (2012).

2. Manolio, T.A. Genomewide association studies and assessment of the risk of disease. N. Engl. J. Med. 363, 166–176 (2010).

3. Maurano, M.T. et al. Systematic localization of common disease-associated variation in regulatory DNA. Science 337, 1190–1195 (2012).

4. Musunuru, K. et al. From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature 466, 714–719 (2010).

5. Bauer, D.E. et al. An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level. Science 342, 253–257 (2013).

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