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dc.contributor.authorGurzadyan, V. G.en_US
dc.contributor.authorYan, H.en_US
dc.contributor.authorVlahovic, G.en_US
dc.date.accessioned2016-10-11T05:37:40Z
dc.date.available2016-10-11T05:37:40Z
dc.date.issued2015en_US
dc.identifier.otherHPU4160562en_US
dc.identifier.urihttps://lib.hpu.edu.vn/handle/123456789/23641en_US
dc.description.abstractThe Kolmogorov–Arnold stochasticity parameter technique is applied for the first time to the study of cancer genome sequencing, to reveal mutations. Using data generated by next-generation sequencing technologies, we have analysed the exome sequences of brain tumour patients with matched tumour and normal blood. We show that mutations contained in sequencing data can be revealed using this technique, thus providing a new methodology for determining subsequences of given length containing mutations, i.e.en_US
dc.format.extent7 p.en_US
dc.format.mimetypeapplication/pdfen_US
dc.language.isoenen_US
dc.subjectGeneticsen_US
dc.subjectBiophysicsen_US
dc.subjectGenomicsen_US
dc.subjectGenome sequencesen_US
dc.subjectCodingen_US
dc.subjectRandomnessen_US
dc.titleDetecting somatic mutations in genomic sequences bymeans of Kolmogorov Arnold analysisen_US
dc.typeArticleen_US
dc.size513KBen_US
dc.departmentEducationen_US


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