Yingying Xia

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Copy-number variations (CNV), loss of heterozygosity (LOH), and uniparental disomy (UPD) are large genomic aberrations leading to many common inherited diseases, cancers, and other complex diseases. An integrated tool to identify these aberrations is essential in understanding diseases and in designing clinical interventions. Previous discovery methods(More)
Voice over IP (VoIP) in LTE-R (LTE for Railway) will replace the circuit-switched (CS) voice service of the GSMR (GSM for Railway). However, it will face new problems in high speed railway scenario. In overlapping areas, the handover signaling (i.e. handover measurement and decision) is of higher priority than Hybrid Automatic Repeat reQuest (HARQ)(More)
Copy-number variations (CNV), loss of heterozygosity (LOH), and uniparental disomy (UPD) are large genomic aberrations leading to many common inherited diseases, cancers, and other complex diseases. An integrated tool to identify these aberrations is essential in understanding diseases and in designing clinical interventions. Previous discovery methods(More)
With the development and clinical application of genomics, more and more concern is focused on single-cell sequencing. In the process of single-cell sequencing, whole genome amplification is a key step to enrich sample DNA. Previous studies have compared the performance of different whole genome amplification (WGA) strategies on Illumina sequencing(More)
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