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Matt Bashton
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Cancer/Clinical Bioinformatician currently working at the Northern Institute for Cancer Research, primarily working with sequencing data from various cancer exomes and genomes - specifically: somatic variant calling (SNVs, indels), structural variant calling and copy number variation. Previously worked/studied: Bioinformatics Support Unit, EMBL-EBI (Thornton group), MRC-LMB (Chothia group), Sanger Institute (Pfam).

Publications: Pubmed, Google Scholar

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