and Genome Analysis in Cancer
Chromosome and Genome Analysis in Cancer We have focused in this chapter on constitutional chromosome abnormalities that are seen in most or all of the cells in the body and…
Chromosome and Genome Analysis in Cancer We have focused in this chapter on constitutional chromosome abnormalities that are seen in most or all of the cells in the body and…
References for Specific Topics Alkan C, Coe BP, Eichler EE. Genome structural variation discovery and genotyping. Nature Rev Genet. 2011;12:363–376. Bagnall RD, Waseem N, Green PM, Giannelli F. Recurrent inversion…
General References Olson MV. Human genetic individuality. Ann Rev Genomics Hum Genet. 2012;13:1–27. Strachan T, Read A. Human molecular genetics. ed 4. Garland Science: New York; 2010. 2012. The 1000…
Impact of Mutation and Polymorphism Although it will be self-evident to students of human genetics that new deleterious mutations or rare variants in the population may have clinical consequences, it…
Variation in Individual Genomes The most extensive current inventory of the amount and type of variation to be expected in any given genome comes from the direct analysis of individual…
Figure 4-4 Examples of mutations in a portion of a hypothetical gene with five codons shown (delimited by the dotted lines). The first base pair of the second codon in the reference…
Figure 3-1 The amplification of genetic information from genome to gene products to gene networks and ultimately to cellular function and phenotype. The genome contains both protein-coding genes (blue) and noncoding RNA…
http://genome.ucsc.edu/cgi-bin/hgGatewayhttp://www.ensembl.org/Homo_sapiens/Info/IndexThe Single Nucleotide Polymorphism Database (dbSNP) and the Structural Variation Database (dbVar) are databases of small-scale and large-scale variations, including single nucleotide variants, microsatellites, indels, and CNVs.http://www.ncbi.nlm.nih.gov/snp/http://www.ncbi.nlm.nih.gov/dbvar/The 1000 Genomes Project…