Associated Papers
Validating Amino Acid Variants in Proteogenomics Using Sequence Coverage by Multiple Reads.
Levitsky LI et al.
Journal of Proteome Research, 2022
35536917 (PubMed )
Supplement: pr2c00033_si_002.pdf
Genetic variation of acquired structural chromosomal aberrations.
Vodicka P et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis, 2018
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Q-01A.domain
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