يعرض 21 - 40 نتائج من 1,081 نتيجة بحث عن '(( ((python two) OR (python tool)) predicted ) OR ( python code implementation ))', وقت الاستعلام: 0.57s تنقيح النتائج
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    ProSmith model overview. حسب Alexander Kroll (9304225)

    منشور في 2024
    الموضوعات:
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    Table_2_BayesPI-BAR2: A New Python Package for Predicting Functional Non-coding Mutations in Cancer Patient Cohorts.docx حسب Kirill Batmanov (3722374)

    منشور في 2019
    "…It is evaluated in follicular lymphoma and skin cancer patients, by focusing on sequence variants in gene promoter regions. BayesPI-BAR2 is a useful tool for predicting functional non-coding mutations in whole genome sequencing data: it allows identification of novel transcription factors (TFs) whose binding is altered by non-coding mutations in cancer. …"
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    Python code that implements the Hoshen Kopleman algorithm used to identify the clusters shown in Figs 9 and 10. حسب Leonardo Costa Ribeiro (10439243)

    منشور في 2023
    "…<p>Python code that implements the Hoshen Kopleman algorithm used to identify the clusters shown in Figs <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0285630#pone.0285630.g009" target="_blank">9</a> and <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0285630#pone.0285630.g010" target="_blank">10</a>.…"
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    PHOTONAI explorer. حسب Ramona Leenings (11167294)

    منشور في 2021
    الموضوعات:
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    Secure Python Code Manager: A Tool for Protected Python Code Distribution and Management حسب Pavel Izosimov (20096259)

    منشور في 2024
    "…</li><li><b>Commercial Distribution</b>: Safely share Python code with clients or customers, implementing advanced <b>Python code protection tools</b> for sales or rentals.…"
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    Table_1_BayesPI-BAR2: A New Python Package for Predicting Functional Non-coding Mutations in Cancer Patient Cohorts.xlsx حسب Kirill Batmanov (3722374)

    منشور في 2019
    "…It is evaluated in follicular lymphoma and skin cancer patients, by focusing on sequence variants in gene promoter regions. BayesPI-BAR2 is a useful tool for predicting functional non-coding mutations in whole genome sequencing data: it allows identification of novel transcription factors (TFs) whose binding is altered by non-coding mutations in cancer. …"