FORMAT OF THE PREDICTIONS ON THE DNA_T DATASET
The predictions for each protein are represented using 8 lines:
1: Protein ID
2: Amino acid sequence
3: Annotations of DNA binding residues (0 for non-binding, 1 for binding, and 2 for unavailable annotation due to missing structure that was excluded from assessment)
4: Comma-separated putative propensities for DNA binding for each residue predicted by BindN+
5: Comma-separated putative propensities for DNA binding for each residue predicted by DBS-PSSM
6: Predicted probilities for DNA binding for each residue predicted by DP-Bind(klr).
7: Comma-separated putative propensities for DNA binding for each residue predicted by DP-Bind(klr)
8: Comma-separated putative propensities for DNA binding for each residue predicted by hybridNAP


FORMAT OF THE PREDICTIONS ON THE RNA_T DATASET
The predictions for each protein are represented using 7 lines:
1: Protein ID
2: Amino acid sequence
3: Annotations of RNA binding residues (0 for non-binding, 1 for binding, and 2 for unavailable annotation due to missing structure that was excluded from assessment)
4: Comma-separated putative propensities for RNA binding for each residue predicted by BindN+
5: Comma-separated putative propensities for RNA binding for each residue predicted by RNABindR
6: Comma-separated putative propensities for RNA binding for each residue predicted by Pprint
7: Comma-separated putative propensities for RNA binding for each residue predicted by hybridNAP


FORMAT OF THE PREDICTIONS ON THE PROTEIN_T DATASET
The predictions for each protein are represented using 6 lines:
1: Protein ID
2: Amino acid sequence
3: Annotations of protein binding residues (0 for non-binding, 1 for binding, and 2 for unavailable annotation due to missing structure that was excluded from assessment)
4: Comma-separated putative propensities for protein binding for each residue predicted by PSIVER
5: Comma-separated putative propensities for protein binding for each residue predicted by SPRINGS
6: Comma-separated putative propensities for protein binding for each residue predicted by hybridNAP