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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
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Genetic Risk ScoreGerm-Line MutationNeoplasms/genetics
- Access Rights
- Application Required
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TEMPO
- Authors
- Biederstedt, EvanXiao, GongyiBolipata, Christopher AllanJonsson, Karl Philip5 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
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DNA Mutational AnalysisGerm-Line MutationMatched-Pair AnalysisSoftware
- Access Rights
- Free to All