Genome & Genetics News from GenomeWeb

Going forward, Complete Genomics will focus on clinical research and support BGI's noninvasive prenatal testing business as well as the launch of its benchtop sequencer in China.

Yakutian horse

Horses in the Siberian Far East appear to have been introduced by the Yakut population within the last several hundred years, adapting to the environment since then.

Cigna worked with InformedDNA to come up with scenarios under which it would cover whole-exome sequencing, although it still considers whole-genome analysis investigational.

Springboarding from his successful crowdfunding campaign, synthetic biologist Josiah Zayner wants to bring molecular biology into everyone's living room.

The Hologic-funded model predicted co-testing would lead to a lifetime savings of $39 per woman, with high cancer detection sensitivity and fewer false positive results.

The company's third quarter revenues jumped nearly 800 percent, in part due to the contribution of PersonalizeDx's urologic cancer testing services.

In PNAS this week: variant protective against Alzheimer's disease, effect of whole-genome duplication on methylation in rice, and more.

Genome editing is also bringing up questions when applied to farm animals, the New York Times reports.

Through a transcriptome study, researchers home in on the activity of inflammation-linked genes in chronically lonely people.

Determining who is and is not an author and where a researcher should fall on a list of authors can be a tricky task, Nature News writes.

Sponsored by
National Center for Biotechnology Information

This webinar highlights important features and demonstrates the practical aspects of using the NCBI BLAST service.

Quantitative real-time PCR (qPCR) is maturing as a technology, becom­ing the central platform and gold standard for much of the molecular research and molecular diagnostics performed today. Behind this success is the field’s increasing awareness of the importance of quality control, validation, and performance assessment.

Lucigen has developed an NGS library technology that generates 20 kb mate pair reads that jump across repetitive elements found in microbial genomes (, which dramatically improves the success of assembly de novo by resolving repeat elements and ordering contigs. Six microbial genomes have been assembled de novo and completely closed and finished using Lucigen’s NxSeq® 20 kb mate pair library kit, a companion fragment library, and SPAdes assembly software.