By Jeffrey C. Hall
The sector of genetics is speedily evolving and new clinical breakthroughs are occuring due to advances in wisdom won from genetics study. This sequence constantly publishes very important stories of the broadest curiosity to geneticists and their colleagues in affiliated disciplines.
Read Online or Download Advances in Genetics, Vol. 62 PDF
Best genetics books
Polyploidy – whole-genome duplication (WGD) – is a primary motive force of biodiversity with major outcomes for genome constitution, association, and evolution. as soon as thought of a speciation method universal purely in vegetation, polyploidy is now well-known to have performed a massive function within the constitution, gene content material, and evolution of so much eukaryotic genomes.
This quantity includes state of the art equipment tackling all features of small non-coding RNAs biology. Small Non-Coding RNAs: tools and Protocols publications readers via personalized committed protocols and applied sciences that would be of important aid to all these prepared to give a contribution decoding the varied features of small non-coding RNAs.
"This name will offer cytogenetic, FISH and microarray laboratory average working methods (SOP's) and knowledge on the way to successfully write SOP's; validation plans and summaries; chemical, protection, quality controls and caliber insurance courses; and plans for potent use of reagents, tools and equipment"--Provided by means of writer.
- The Gene Wars: Science, Politics, And The Human Genome
- Pseudogenes: Functions and Protocols
- Born That Way: Genes, Behavior, Personality
- The Torn Timeline
- Population Genetics
- Eugenics: a very short introduction
Additional resources for Advances in Genetics, Vol. 62
High level of functional polymorphism indicates a unique role of natural selection at human immune system loci. Immunogenetics 57, 821–827. Hunter, D. J. (2005). Gene–environment interactions in human diseases. Nat. Rev. 6, 287–298. Hunter, D. , Khoury, M. , and Drazen, J. M. (2008). Letting the genome out of the bottle—will we get our wish? N. Engl. J. Med. 358, 105–107. Hunter, D. , Jacobs, K. , Cox, D. , Hankinson, S. , et al. (2007a). A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.
O’Dwyer, P. , and Catalano, R. B. (2006). Uridine diphosphate glucuronosyltransferase (UGT) 1A1 and irinotecan: Practical pharmacogenomics arrives in cancer therapy. J. Clin. Oncol. 24, 4534–4538. Offit, K. (2008). Genomic profiles for disease risk: Predictive or premature? JAMA 299, 1353–1355. Ott, J. (1999). Methods of analysis and resources available for genetic trait mapping. J. Hered. 90, 68–70. Packer, B. , et al. (2006). SNP500 Cancer: A public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.
J. Hum. Genet. 78, 437–450. , Altman, W. , Bader, J. , Bemben, L. , Braverman, M. , Chen, Y. , Dewell, S. , et al. (2005). Genome sequencing in microfabricated high-density picolitre reactors. Nature 437, 376–380. , Kennedy, G. , et al. (2004a). Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays. Nat. Methods 1, 109–111. , Tsai, Y. , Liu, W. , Kennedy, G. , et al. (2004b). Parallel genotyping of over 10,000 SNPs using a oneprimer assay on a high-density oligonucleotide array. Genome Res.
Advances in Genetics, Vol. 62 by Jeffrey C. Hall