Associated Papers
Refined variant calling pipeline on RNA-seq data of breast cancer cell lines without matched-normal samples.
Eberth S et al.
Bmc Research Notes, 2025
39955561 (PubMed )
Supplement: 13104_2025_7140_MOESM3_ESM.xlsx › snv_indel_maf_less20_Project_bc
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification.
Tretter C et al.
Nature Communications, 2023
37532709 (PubMed )
Supplement: 41467_2023_39570_MOESM4_ESM.xlsx › shared_somatic_mut._min4
Clinical and Genetic Analysis of CHD7 Expands the Genotype and Phenotype of CHARGE Syndrome.
Qin Z et al.
Frontiers in Genetics, 2020
32625235 (PubMed )
Supplement: Data_Sheet_1.zip › Supplementary_Table_2.XLSX › patient_1
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