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  • Anonymized germline variants of prospectively characterized clinical cancer specimens

    Authors
    Berger, Michael Forman
    Description

    Description from dbGaP: "These clinical specimens represent solid tumors and matched blood controls that were collected as part of patients' routine care at Memorial Sloan Kettering Cancer Center. They were sequenced on the targeted platform MSK-IMPACT. Here, we performed germline variant calling on the normal blood specimens and assessed their zygosity in the concomitant tumor specimens for comprehensive...

    Subject
    Genetic Risk Score
    Germ-Line Mutation
    Neoplasms/genetics
    Access Rights
    Application Required
  • TEMPO

    Authors
    Biederstedt, Evan
    Xiao, Gongyi
    Bolipata, Christopher Allan
    Jonsson, Karl Philip
    5 more author(s)...
    Description

    Description from GitHub: "Tempo is a CMO Computational Sciences (CCS) research pipeline processing WES & WGS tumor-normal pairs using the Nextflow framework. Currently the pipeline is composed of alignment and QC, and detection of both somatic alterations and germline variants. Users can begin with inputs of either paired-end FASTQs or BAMs, and process these via the command line. For further details...

    Subject
    DNA Mutational Analysis
    Germ-Line Mutation
    Matched-Pair Analysis
    Software
    Access Rights
    Free to All