Next Generation sequencing

  1. PacBio Sequel: Scaling Up SMRT Technology

    The major advantage of SMRT sequencing over other technologies is the long read-length. Other major benefits of the platform, such as improved de novo assembly and detection of structural variation are derived from this advantage. With more and more evidence pointing to the importance of structural variation between different genomes, PacBio’s long reads put it in a unique market position.

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  2. NGS RNA-Seq

    While a lot of useful information can be gleaned from analyzing DNA, it can represent a somewhat static view of the organism. Outside of somatic mutations, DNA sequences change very little throughout the organism’s life cycle. Life is very dynamic by nature - being able to explore the constant change happening as an organism responds to its environment is a crucial part of the whole picture.

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  3. Metagenomics Analysis

    Metagenomics is a very broad field that can often be summarized down to the analysis of a microbiome. These microbiomes are all around and inside us. They’re in the air we breathe, the water we drink and the food we eat.

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  4. Human Whole Genome Sequencing

    The genome is the unique blueprint of every living organism on earth. In almost every other species like humans, exhaustive research has demonstrated it is also in concert with environmental and epigenetic factors. Changes in it, is undeniably one of the pillars of disease pathogenesis - or lack thereof.
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  5. Whole Exome Sequencing

    For many projects, it can be overkill to do Whole Genome Sequencing (WGS). Projects with a more specific focus can leverage Whole Exome Sequencing (WES), thanks to its higher coverage and lower overall cost.
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  6. Buying vs Outsourcing Sequencing Platforms

    The advent of next-generation sequencing has revolutionized biology and many other fields. Sequencing is now used to develop new drugs, understand personal ancestry and predisposition to certain diseases, improve yields in agriculture, find new oil fields, and in many other areas. DNA sequencing is becoming as indispensable as computing in many industries.  

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  7. Navigating Variability of NGS Pricing

    When you are looking for a sequencing facility there are two main factors to consider aside from the quality of the data cost and turn-around time (TAT).  We've researched many facilities across the globe and this is what we have found:

    First, the cost of sequencing varies widely between facilities. In part, this is due to the facility's source of funding: governmental or private. Most government funded academic institutions run their sequencers at cost for their internal users (students and professors). They usually have a pricing structure as follows: cheapest for internal, more expensive for external nonprofit users and the most expensive (sometimes as much as a 50% surcharge) for external for-profit users. To illu

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  8. Demystifying NGS Outsourcing: Aligning Resources, Expertise, and Needs



    The goal of the modern genomics researcher is not simply to build genomics tools or even to gather genomic data. Instead, the ultimate objective is to further scientific knowledge to better understand human disease, plant and animal genetics, microbial ecology or evolution. The genomics researcher or bioinformatician seeks a deeper understanding of the science; better research tools are only a means to this end. A number of complex steps are involved in genomic sequencing, including platform or vendor selection, sample preparation, sequencing, data management and bioinformatics. Each of these individual processes bears its own learning curve, and a failure at any step could cripple downstream results. Next Generati

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  9. Next Generation Sequencing - Overview and Solutions to Common Problems


    Current Next-Generation Sequencing (NGS) platforms employ massively parallel, automatable sequencing approaches designed for maximum output and efficiency. With vastly improved speed and efficiency, modern NGS platforms have enabled an entirely new paradigm for genomic research, with new applications in human disease, small-genome species, metagenomics, consumer testing and more. Early NGS innovations

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