Associated Papers
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
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Supplement: HUMU-36-903-s001.zip › humu22825-sup-00010-Table_S13.xlsx › Sheet1
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
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Patient-derived glioblastoma organoids reflect tumor heterogeneity and treatment sensitivity.
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