News & Events

NGRL Manchester has expanded the functionality of its popular primer checking tool with the launch of SNPCheck v2.1. This version introduces a number of new features including the ability to filter variants from results. The changes have been made in order to address the problem of ‘SNP overload’ created by the rapid expansion of dbSNP over the last year.
 
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SIFT is currently unavailable at sift.jcvi.org while maintenance is performed on the site. We are assured by JCVI that it will be restored as soon as possible. In the meantime the old SIFT website is available at http://blocks.fhcrc.org/sift/SIFT.html. Read on for a quick guide on how to use this version>>
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AstraZeneca has sponsored the development of the Diagnostic Mutation Database (DMuDB) into a National UK Database of variants in the EGFR gene associated with non-small cell lung cancer (NSCLC) tumours. The database will provide clinical, treatment and outcome data for patients  and offers support to laboratories for the interpretation of variants found in the EGFR gene. This testing is used to indicate sensitivity to EGFR-TKIs (e.g. IRESSA).

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This two day interactive workshop is designed specifically for clinical geneticists who wish to gain or update their awareness and practical experience of bioinformatics tools and resources.

The workshop aims to give hands-on experience with clinically useful bioinformatics programs. Interpretation of array findings and single gene variants will be covered.
More information >>

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This two day interactive workshop is aimed specifically at trainee staff who wish to gain or update their knowledge and practical experience of bioinformatics tools and resources in light of the increasing use of computers in the molecular and cytogenetics laboratory.
More information >>

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