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New Product Watch: Dec 9, 2008

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InfoQuant last week launched oneClickCGH and CGH Fusion version 5.0. The London-based firm's new software packages allow the integration of loss-of-heterozygosity and copy number data with data from SNP arrays.
 
Specifically, oneClickCGH 5.0 provides integrated genome-wide CNV frequencies, the construction of interactive custom CNV tracks, gene significance analysis, integrated Progenetix CGH data, and allele-specific plots for LOH detection.
 
CGH Fusion 5.0 enables batch-mode copy number and LOH detection, simultaneous visualization of multiple samples, joint log-ratio and allele-specific plots, comprehensive aberration report formats, and interactive cross-sample alteration frequency profiles.

The Scan

Researchers Compare WGS, Exome Sequencing-Based Mendelian Disease Diagnosis

Investigators find a diagnostic edge for whole-genome sequencing, while highlighting the cost advantages and improving diagnostic rate of exome sequencing in EJHG.

Researchers Retrace Key Mutations in Reassorted H1N1 Swine Flu Virus With Avian-Like Features

Mutations in the acidic polymerase-coding gene boost the pathogenicity and transmissibility of Eurasian avian-like H1N1 swine influenza viruses, a PNAS paper finds.

Genome Sequences Reveal Evolutionary History of South America's Canids

An analysis in PNAS of South American canid species' genomes offers a look at their evolutionary history, as well as their relationships and adaptations.

Lung Cancer Response to Checkpoint Inhibitors Reflected in Circulating Tumor DNA

In non-small cell lung cancer patients, researchers find in JCO Precision Oncology that survival benefits after immune checkpoint blockade coincide with a dip in ctDNA levels.