Genome & Genetics News from GenomeWeb

The Sequel system, which was developed as part of PacBio's collaboration with Roche, will have seven times the throughput of the RS II and cost $350,000.

Color Genomics hopes its recently launched benefits program will enable a broader population to have access to breast and ovarian cancer risk testing.

The firm's EmbryVu test is based on an NGS method it licensed from Johns Hopkins University last year, called FAST-SeqS.

Specific proposals would negatively impact independent labs and labs with algorithm-based tests, while some interpretations don't align with statutory language, experts said.

Scientists at CSHL's Genome Engineering meeting offered their thoughts on the Zhang Lab's discovery published Friday in Cell.

The test is for determining whether a patient's tumor expresses the PD-L1 protein and is likely to respond to Merck's drug Keytruda, which the FDA also approved today.

In Science this week: certain genes repressed during memory formation, analysis of genomes from single neurons, and more.

NASA plans to test whether DNA sequencing studies can be conducted in microgravity.

Congress passes a continuing resolution to keep the US federal government funded through mid-December.

The Human Genome Project was launched 25 years ago, and at Nature, Francis Collins, James Watson, and Eric Green look back at the lessons learned.

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.