Publication | Open Access

Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer

Functional GenomicsSequencingSingle Cell SequencingMedicineGeneticsSingle Nucleotide VariantsNext-generation SequencingWhole ExomePathologyCancer GenomicsGenomicsMolecular DiagnosticsBioinformaticsLung CancerVariant Interpretation