VarDictJava software on GitHub in support of 'A benchmarking study of individual somatic variant callers and voting-based ensembles for whole-exome sequencing'

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VarDictJava software on GitHub

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Abstract

VarDict Java port

9 Research products, page 1 of 1

Integrated bioinformatic pipeline using whole-exome and RNAseq data to identify germline variants correlated with cancer
2022IsRelatedTo
Clonal dynamics and somatic evolution of haematopoiesis in mouse
2024IsRelatedTo
Clonal dynamics and somatic evolution of haematopoiesis in mouse
2025IsRelatedTo
Additional file 1 of Integrated approach to generate artificial samples with low tumor fraction for somatic variant calling benchmarking
2024IsRelatedTo
Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing
2021IsRelatedTo
A benchmarking study of individual somatic variant callers and voting-based ensembles for whole-exome sequencing
2024IsRelatedTo
Diseño de un flujo de trabajo para el análisis de datos procedentes de secuenciación masiva
2021IsRelatedTo
VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research
2016IsRelatedTo
Tumor cell enrichment by tissue suspension enables detection of mutations with low variant allele frequency and estimation of germline mutations
2022IsRelatedTo