TABLE V.
Tool | -Omic Data | -Omic Biomarker | Approach |
---|---|---|---|
SNPassoc [89] | Genomic | Significant SNPs associated with traits |
Genome- wide association studies |
SNPTEST* [90] | |||
VAT [91] | Significant SNPs and indels associated with traits |
||
PLINK* [92] | Significant SNPs, indels, and CNVs associated with traits |
||
CNVRuler [93] | Significant CNVs associated with traits |
||
edgeR* [94] | Transcriptomic | Differentially expressed genes /transcripts |
Differential analysis (model fitting and statistical tests) |
DESeq2* [95] | |||
omniBiomarker [96] | |||
DiffSplice [97] | Differential alternative splicing |
||
MATS [98] | |||
DBChIP [99] | Epigenomic | Differential binding sites | |
ChIPDiff [100] | Differential histone modification sites |
||
QDMR [101] | Differentially methylated regions |
||
DetectTLC [102] | Proteomic and metabolomic |
Molecular patterns in mass spectrometry images |
Similarity scoring |
Automics [103] | Differentially abundant metabolites |
Supervised and unsupervised learning |
|
MetaboAnalyst* [104] |
SNPassoc stands for SNP-based whole genome association studies; VAT, variant association tools; PLINK, population-based linkage analyses; edgeR, empirical analysis of digital gene expression data in R; MATS, multivariate analysis of transcript splicing; DBChIP, differential binding with ChIP-seq data; and QDMR, quantitative differentially methylated regions.
Highly impactful tool with more than 50 citations per year.