Daniel Nilsson · researcher (ORCID 0000-0001-5831-385X) · YYNN

Daniel Nilsson

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researcher (ORCID 0000-0001-5831-385X)

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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

scientific article

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

scientific article published on 07 November 2019

pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing

scientific article published on 03 April 2020

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