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Supplement: supplement_1.xlsx › SNVs
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Supplement: 12881_2020_1087_MOESM1_ESM.xlsx › HL1
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Supplement: 41598_2018_34262_MOESM2_ESM.xlsx › 2._minor_allele_frequency_1
ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories.
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Supplement: 13073_2015_207_MOESM1_ESM.xlsx › S6
Identification of HPV integration and gene mutation in HeLa cell line by integrated analysis of RNA-Seq and MS/MS data.
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Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas.
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Nature Communications, 2015
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Supplement: ncomms7044-s3.xlsx › Supplementary_Data_2
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