1 |
A. Park. (2012. Sep). Junk DNA - Not So Useless After All. TIME.
|
2 |
D. Vendramini. (2004). Noncoding DNA and Teem Theory of Inheritance, Emotions and Innate Behavior. Medical Hypotheses 64(3), 512-519. DOI : 10.1016/j.mehy.2004.08.022
DOI
|
3 |
The International SNP Map Working Group. (2001). A map of human genome sequence variation containing 1.42 million single nucelotide polymorphisms. Nature 409, 928-933.
DOI
|
4 |
The International HapMap Consortium. (2005). A haplotype map of the human genome. Nature. 437(7063), 1299-1320. DOI : 10.1038/nature04226
DOI
|
5 |
Q. Chen & F. Sun. A unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms. BMC Genomics, 14(1). DOI : 10.1186/1471-2164-14-S1-S1
DOI
|
6 |
L. B. Barreiro, G. Laval, H. Quach, E. Patin & L. Quintana-Murci. (2008). Natural selection has driven population differentiation in modern humans. Nature Genetics. 40(3), 340-345. DOI : 10.1038/ng.78
DOI
|
7 |
O. Harismendy et al. (2010). Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level. Genome Biology, 11(11), R118. DOI : 10.1186/gb-2010-11-11-r118
DOI
|
8 |
T. A. Manolio. (2010). Genomewide association studies and assessment of the risk of disease. The New England Journal of Medicine. 363(2), 166-76. DOI : 10.1056/NEJMra0905980
DOI
|
9 |
S. Raychaudhuri et al. (2009). Identifying Relationships among Genomic Disease Regions: Predicting Genes at Pathogenic SNP Associations and Rare Deletions. PLoS Genetics, 5(6), e1000534. DOI : 10.1371/journal.pgen.1000534
DOI
|
10 |
B. Bandyopadhyay, V. Chanda & Y. Wang. (2017). Finding the Sources of Missing Heritability within Rare Variants Through Simulation. Bioinform Biol Insights. DOI : 10.1177/1177932217735096
DOI
|
11 |
R. Chenna et al. (2003). Multiple sequence alignment with the Clustal series of programs. Nucleic Acids Research, 31(13), 3497-500. DOI : :10.1093/nar/gkg500
DOI
|
12 |
D. B. Goldstein, A. Allen, J. Keebler, E. H. Margulies, S. Petrou, S. Pertrovski & S. Sunyaev. (2013). Sequencing studies in human genetics: design and interpretation. Nature Reviews Genetics, 14(7), 460. DOI : 10.1038/nrg3455
DOI
|
13 |
C. S. Carlson, M. A. Eberle, L. Kruglyak & D. A. Nickerson. (2004). Mapping complex disease loci in whole-genome association studies. Nature, 429(6990), 446-452. DOI : 10.1038/nature02623
DOI
|
14 |
S. C. Schuster. (2007). Next-generation sequencing transforms today's biology. Nature Methods, 5(1), 16-18. DOI : 10.1038/nmeth1156
DOI
|
15 |
E. Pennisi. (2012). ENCODE Project Writes Eulogy for Junk DNA. Science, 337(6099), 1159-1161 DOI : 10.1126/science.337.6099.1159
DOI
|
16 |
B. Carlson. (2008. June). SNPs - A Shortcut to Personalized Medicine. Genetic Engineering & Biotechnology News, 28(12).
|
17 |
T. A. Manolio. (2010). How to interpret a genome-wide association study. JAMA. 363(2), 166-76. DOI : 10.1001/jama.299.11.1335
|
18 |
A. J. Davison & J. E. Scott. (1986). The complete DNA sequence of varicella-zoster virus. Journal of General Virology, 67(Pt9), 1759-1816. DOI : 10.1099/0022-1317-67-9-1759
DOI
|