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SeqPlus – A novel method for FFPE sample analysis

Presentation of AstraZeneca's findings that our SeqPlus gives improved coverage of genes from FFPE samples, enabling more efficient exome sequencing.

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February 7, 2018

Experiencing Variant Science – a new approach for clinicians

Kirk Brote will discuss the tools available for use when researching variant science. There is a growing need for teams to work more collaboratively and produce consistent, valid, and repeatable work.

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November 9, 2017

Interactive Analysis and Visualization of TCGA Tumor Datasets using the WuXi NextCODE system

This talk will demonstrate how to replicate and extend published analysis on TCGA datasets including driver gene analysis.

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September 19, 2017

Using the GORpipe genomic query language: “many small sharp tools” for big data analysis

Join us as we showcase a workflow for bioinformaticians to conduct their own genomic analyses using our highly flexible query tool, GORpipe, on their local machine.

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August 17, 2017

Exploring high-quality whole-genome sequencing of FFPE samples from a large cancer cohort

Hear Shannon Bailey present the results from a large cancer sequencing project where WuXi NextCODE's method was used to generate high-quality WGS data from FFPE tumor-normal sample pairs.

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August 3, 2017

Small screens, big ambitions: What place do mobile apps have in genomic research

More and more researchers need the ability to access information wherever and whenever. Enter mobile devices.

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July 27, 2017

The Use of Clinical Sequence Analyzer (CSA) to Explore Genomic Data on Rare Diseases

Hear the journey of a six year old male with dysmorphic features, developmental delays, and speech regression from initial presentation to final diagnosis.

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Genomics Medicine Ireland is also hiring a wide range of scientific, partnership and support roles in the field of genomics.

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