Deletions, duplications or rearrangements of genomic regions in the human genomes produce differences in gene copy numbers, referred to as copy number variations (CNV). Those variations account for a ...

Although array comparative genomic hybridization (aCGH) is currently established as the gold standard for copy number variation (CNV) detection, next-generation sequencing (NGS) is increasingly being ...

Findings published today in Science will accelerate the search for genes involved in human disease. The report provides a first genome-wide view of how the unique composition of genetic variation ...

Findings published in Science will accelerate the search for genes involved in human disease. This first genome-wide view shows that activity of more than 1000 genes is affected by sequence variation.

They also used an Affymetrix gene-expression array to profile the transcriptome of six different tissues. Reymond described significantly greater variation of gene expression for genes located in a ...

Copy Number Variation CNV: is a phenomenon in which divisions of the genome are repeated and the number of repeats in the genome varies between individuals in the human population.

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Universal Diagnostics (Universal DX), a bioinformatics and multi-omics company on a mission to transform cancer into a curable disease, today announced the results ...

Comprehensive genomic profiling (CGP) in post-systemic treatment (Post) metastatic sites (MET) and pretreatment (Pre) primary tumors (PT) of metastatic prostate cancer (mPC).

A prospective comparison of ER, PR, Ki67 and gene expression in paired sequential core biopsies of primary, untreated breast cancer. This is an ASCO Meeting Abstract from the 2015 ASCO Annual Meeting ...