Latest resources

Many single nucleotide polymorphisms (SNPs) have been identified in the human genome. These normal variations have been particularly useful in the study of loss of heterozygosity (LOH) in cancer, in linkage studies of patterns of familial inheritance and in the search for low penetrance genes associ ...
Array based chromosomal genomic hybridisation (array CGH) has dramatically increased the level of resolution for detection of DNA copy number alterations. Further challenges now emerge through the simultaneous availability of transcriptome, miRNAome and epigenome profiles. One particular daunting ta ...
Array Comparative Genomic Hybridization (array CGH) is the high-resolution laboratory technique of choice for the detection of chromosomal DNA copy number aberrations on a genome-wide scale (Costa et al., 2008). To perform array CGH initially PCR amplified bacterial artificial chromosomes (BACs) or ...
MicroRNAs are an emerging class of small non-coding RNAs implicated in a wide variety of biological and cellular processes. Research in this field is accelerating and the growing number of miRNAs emphasizes the need for high throughput and sensitive detection methods. We present the successful evalu ...
Array Comparative Genomic Hybridization (array CGH) is the high-resolution laboratory technique of choice for the detection of chromosomal DNA copy number aberrations on a genome-wide scale (Costa et al., 2008). To perform array CGH initially PCR amplified bacterial artificial chromosomes (BACs) or ...
sfy39587f01