Publication | Open Access

Best practices for benchmarking germline small-variant calls in human genomes

BioinformaticsLong-read SequencingMedicineGeneticsComputational GenomicsNext-generation SequencingStatistical GeneticsHigh Throughput SequencingBiostatisticsGenetic VariationGenomicsPublic HealthPopulation GeneticsFunctional GenomicsHuman Genomes