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    Genome Canada and its partners recently funded two new initiatives with C$255 that will back precision medicine, genomics, and technology development.

    The partners will integrate genomic, imaging, and other data to identify new therapies and personalize treatments for patients with neurological and neurodegenerative diseases.

    Qiagen GeneReader Users Present Early Results at AMP Global Congress

    Article: In-Depth—in Molecular Diagnostics

    Groups from Austria, Spain, Germany, and the US demonstrated that the GeneReader can reliably detect cancer mutations in tissue and liquid biopsy samples.

    PointCross Life Sciences Emerges From Stealth to Wrangle Data for Drug Developers

    Article: In-Depth—in Informatics

    The firm is counting on its experience integrating data from the oil and gas industry to change the way pharmaceutical data scientists work.

    UBC Group Debuts Single-Cell Sequencing Method Without Whole Genome Amplification

    Article: In-Depth—in Sequencing

    The method allows analysis of copy number at the individual cell level with greater coverage uniformity and more reliable detection than other approaches.

    New bioinformatics businesses bloomed over the past year in spite of a challenging market and encroachment from instrument vendors and other larger entities.

    Canada's Cyclica Targets Pharma with Drug-Protein Interaction Search Software

    Article: In-Depth—in Informatics

    The company's Ligand Express software combines biological, chemical, and protein structure data to identify candidate molecules for further research and development. 

    10X's approach is a synthetic long-read technology that leverages existing short-read NGS technology but fills in knowledge gaps about the human genome.

    BioInnovation Solutions, formerly Pathogenica, and Enzymatics are developing a rapid Ebola diagnostic and have validated it on patient samples in Nigeria.

    NEW YORK (GenomeWeb) – The University of California, Santa Cruz has received $11 million in grant funding from the National Institutes of Health to support the establishment of a so-called Center for Big Data in Translational Genomics, a multi-institutional collaboration based at UCSC, and to dev

    Cellular Research, Seven Bridges Partner to Offer RNA-seq Products

    Article: Breaking News—in Microarrays & Multiplexing

    NEW YORK (GenomeWeb) — Cellular Research said today that it is collaborating with Seven Bridges Genomics to provide customers with a "complete analysis pipeline" to run RNA sequencing experiments.

    NEW YORK (GenomeWeb) – The National Institutes of Health has approved a proposal to develop a framework that will connect biomedical data, software, training materials, and other resources developed as part of NIH-funded research projects, making them more accessible and shareable.

    NEWYORK (GenomeWeb) – Newly minted health data startup SolveBio is seeking to build a business based on its informatics platform to help scientists developing diagnostic and research applications in hospitals, academia, and industry access and use genomic and other kinds of data more easily.

    ABRF Panelists Discuss NIH Efforts for Sharing Big Data

    Article: Breaking News—in Informatics

    ALBUQUERQUE, NM (GenomeWeb News) — The rate at which data are being produced shows no signs of slowing and, according to Philip Bourne, the new associate director for data science at the National Institutes of Health, is still increasing.

    Illumina announced a new automated sequencing library prep system called NeoPrep last week, along with plans to sell customized versions of the MiSeq system for forensics and HLA typing.

    CHOP's Harvest Toolkit Offers Reusable Components for Biomedical Data Exploration

    Article: In-Depth—in Informatics

    A team of informatics experts and biomedical researchers at the Children's Hospital of Pennsylvania has developed a general framework called Harvest that provides bioinformatics developers with reusable tools to creat

    Natera Plans Test Expansion as It Reports Clinical Data; User Details Experiences

    Article: In-Depth—in Clinical Sequencing

    With the launch of its noninvasive sequencing-based prenatal aneuploidy test in March, Natera became the latest company to enter the highly competitive space, which includes first-comer Sequenom, Illumina-owned Verinata Health, and Ariosa Diagnostics.

    Building on a targeted sequencing method that uses molecular inversion probes to capture and sequence genes, researchers at the University of Washington have added a single-molecule tagging component to reduce the sequencing error rate and enable the detection of low-frequency va

    The results of Boston Children's Hospital's Children's Leadership Award for the Reliable Interpretation and appropriate Transmission of Your genomic information, or CLARITY, contest suggest that the community largely agrees on the best informatics approaches for clinical genomic

    Informatics startup Code-N has launched an early-access program that will allow pharmaceutical companies to test-drive Green Field Finder, its cloud-based semantic software that helps researchers search the patent databases to assess the competitive opportunity for drug candidate


360Dx reports that the US Centers for Medicare & Medicaid Services would cover next-generation sequencing-based cancer panel tests.

The Washington Post reports that a meteorologist is being considered as presidential science and technology advisor.

In PNAS this week: precision medicine strategy to screen for disease risk, genome evolution in Haemophilus influenzae, and more.

Researchers have developed a PCR-based assay to gauge whether manatees are present in waters.