Global ETD Search

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Showing 1 to 3 of 3 for “"Error-corrected sequencing"”.

  1. EVALUATION OF THE RISK OF SECONDARY LEUKEMIAS IN CANCER SURVIVORS

    … chemotherapy. We used high-sensitivity error-corrected sequencing (limit of sensitivity VAF>0.1%) for CH analysis, in order to detect mutations well below the cutoff of the clinical threshold of CHIP (variant allele frequency (VAF) >2%). In both cohorts, pathogenic germline mutations …

    milano Repository record for EVALUATION OF THE RISK OF SECONDARY LEUKEMIAS IN CANCER SURVIVORS (opens in a new tab)

  2. Investigating clonal hematopoiesis in rhesus macaque and human

    … of hematological malignancies, recent large deep sequencing studies have revealed that clonally-expanded HSPC with specific somatic mutations are also prevalent in individuals without overt hematological abnormalities and become increasingly common with age. The phenomenon is thus termed …

    cambridge Repository record for Investigating clonal hematopoiesis in rhesus macaque and human (opens in a new tab)

  3. The evolutionary dynamics of clonal haematopoiesis and its progression to acute myeloid leukaemia

    … haematopoiesis driver mutation. Using blood sequencing data amassed from ~50,000 individuals, combined with insights from evolutionary theory, we developed a framework to quantify the mutation rates and fitness effects of clonal haematopoiesis variants down to single nucleotide resolution. …

    cambridge Repository record for The evolutionary dynamics of clonal haematopoiesis and its progression to acute myeloid leukaemia (opens in a new tab)