Publication | Closed Access
Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases
30
Citations
12
References
2018
Year
Pair AnalysisGeneticsGenetic EpidemiologyMolecular GeneticsGenomicsHigh Throughput SequencingCopy Number VariationsBiostatisticsPublic HealthPersonal GenomicsVariant InterpretationInherited Kidney DiseasesSequence AnalysisStatistical GeneticsSequencingFunctional GenomicsBioinformaticsNext-generation SequencingMedicine
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