Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
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Updated
Jan 27, 2020 - Nextflow
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Flujos de trabajos desarrollados y automatizados en el Inmegen para el procesamiento de datos genómicos y transcriptómicos.
Detect germline or somatic variants from normal or tumour/normal whole-genome, whole exome, or targeted sequencing with high performance computing.
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