Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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P1476

Personal Cancer Genome Reporter: variant interpretation report for precision oncology.

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P2093

Daniel Vodák

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Ghislain Fournous

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Lars Birger Aasheim

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DoCM: a database of curated mutations in cancer.

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Somatic cancer variant curation and harmonization through consensus minimum variant level data

IntOGen-mutations identifies cancer drivers across tumor types.

Oncotator: cancer variant annotation tool.

DGIdb 2.0: mining clinically relevant drug-gene interactions.

DeconstructSigs: delineating mutational processes in single tumors distinguishes DNA repair deficiencies and patterns of carcinoma evolution

Vcfanno: fast, flexible annotation of genetic variants

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1778-1780

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scholarly article

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10.1093/BIOINFORMATICS/BTX817

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English

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P478

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P50

Ola Myklebost

Eivind Hovig

Sigve Nakken

P577

2018-05-01T00:00:00Z

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P698

29272339

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5946881

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