Publication | Open Access

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

Long-read SequencingHaplotype DeterminationAllelic VariantSequencingNext-generation SequencingGeneticsGenetic EpidemiologyClinical Sequencing ApplicationsStatistical GeneticsGenetic VariationGenomicsPublic HealthSystems BiologyMedicineBioinformaticsHaplotype-based ApproachesVariant Interpretation