From: A review of deep learning applications in human genomics using next-generation sequencing data
Tools | DL model | Application | Input/Output | Website Code Source | References |
---|---|---|---|---|---|
DeepSEA | CNN | To predict multiple chromatin effects of DNA sequence alterations | N/A | [165] | |
FactorNet | CNN + RNN | For predict the cell-type specific transcriptional binding factors (TF) | BED / BED, gzipped bedgraph file | [120] | |
DeMo (Deep Motif Dashboard) | CNN + RNN | For transcription factor binding site perdition (TFBS) by classification task | FASTA / txt | [166] | |
DeepCpG | CNN + GRU | To predict the methylation states from single-cell data | TSV / TSV | [83] | |
DeepHistone | CNN | To accurately predict histone modification sites based on sequences and DNase-Seq (experimental) data | txt, CSV / CSV | [84] | |
DeepTACT | CNN | To predict 3D chromatin interactions | CSV / CSV | [167] | |
Basenji | CNN | To predict cell-type-specific epigenetic and transcriptional profiles in large mammalian genomes | FASTA / VCF | [114] | |
Deopen | CNN | To predict the chromatin accessibility from DNA sequence/ Downstream analysis also included QTL analysis | BED, hkl /hkl | [31] | |
DeepFIGV (Deep Functional Interpretation of Genetic Variants) | CNN | To predicts impact on chromatin accessibility and histone modification | FASTA / TSV | [62] |