Sökning: "Mutation testing"

Visar resultat 1 - 5 av 56 avhandlingar innehållade orden Mutation testing.

  1. 1. A Mutation-based Framework for Automated Testing of Timeliness

    Författare :Robert Nilsson; Sten F. Andler; Michael G. Hinchey; Linköpings universitet; []
    Nyckelord :NATURAL SCIENCES; NATURVETENSKAP; NATURVETENSKAP; NATURAL SCIENCES; Automated Testing; Timeliness; Real-time systems; Time constraints; Model-based; Mutation testing; Computer science; Datalogi;

    Sammanfattning : A problem when testing timeliness of event-triggered real-time systems is that response times depend on the execution order of concurrent tasks. Conventional testing methods ignore task interleaving and timing and thus do not help determine which execution orders need to be exercised to gain confidence in temporal correctness. LÄS MER

  2. 2. Automating Black-Box Property Based Testing

    Författare :Jonas Almström Duregård; Chalmers University of Technology; []

    Sammanfattning : Black-box property based testing tools like QuickCheck allow developers to write elegant logical specifications of their programs, while still permitting unrestricted use of the same language features and libraries that simplify writing the programs themselves. This is an improvement over unit testing because a single property can replace a large collection of testcases, and over more heavy-weight white-box testing frameworks that impose restrictions on how properties and tested code are written. LÄS MER

  3. 3. Methodological aspects and usefulness of Quantitative Sensory Testing in early small fiber polyneuropathy : a clinical study in Swedish hereditary transthyretin amyloidosis patients

    Författare :Victoria Heldestad; Erik Nordh; Ole Suhr; Göran Solders; Umeå universitet; []
    Nyckelord :MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Amyloidosis; cold thresholds; heart rate variability; method-of-limits; quantitative sensory testing; transthyretine; warm thresholds; Clinical Neurophysiology; klinisk neurofysiologi;

    Sammanfattning : Generalised polyneuropathy (PNP) is a common cause to neurological impairment, and may be an early symptom of a severe systemic disease. One such illness is hereditary transthyretin (TTR) amyloidosis (ATTR), a progressive fatal disorder caused by a mutation on the TTR gene. LÄS MER

  4. 4. Application of In Vitro Chemosensitivity Testing for Evaluation of New Cytotoxic Drugs in Chronic Lymphocytic Leukaemia

    Författare :Anna Åleskog; Jan Liliemark; Uppsala universitet; []
    Nyckelord :MEDICAL AND HEALTH SCIENCES; MEDICIN OCH HÄLSOVETENSKAP; MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Clinical drug development; chronic lymphocytic leukaemia; cytotoxicity; in vitro assay; cytotoxic drug development; CHS 828; IgVH mutation status; Klinisk läkemedelsutveckling; Pharmaceutical chemistry; Läkemedelskemi; Clinical Pharmacology; klinisk farmakologi;

    Sammanfattning : Despite major advances in the understanding of the biology of chronic lymphocytic leukaemia (CLL), progress in improving its treatment has been limited and it still remains an incurable disorder. In the present research, we have performed in vitro drug sensitivity testing of primary CLL cells for preclinical evaluation of cytotoxic drugs, using the fluorometric microculture cytotoxicity assay (FMCA). LÄS MER

  5. 5. Hereditary breast/ovarian cancer : Implementation of BRCA1 & BRCA2 testing

    Författare :Brita Arver; Karolinska Institutet; Karolinska Institutet; []

    Sammanfattning : Breast cancer is the most common malignancy among women in the western world. Most cases are sporadic but in 5 to 10 % an inherited genetic mutation is the main cause of the disease. LÄS MER