Data used in our mini-benchmark.
Input files can be found in:

<table>
  <tr>
    <th>Sequence category</th>
    <th>File</th>
  </tr>
  <tr>
    <td>coding transcripts</td>
    <td>Supplement/sampled_sequences/coding_sample.fa</td>
  </tr>
  <tr>
    <td>lncRNA transcripts</td>
    <td>Supplement/sampled_sequences/lncRNA_sample.fa</td>
  </tr>
  <tr>
     <td>mononucleotides sequences</td>
    <td>Supplement/sampled_sequences/randomized_sample.fa</td>
  </tr>
  <tr>
     <td>random genomic sequences</td>
    <td>Supplement/sampled_sequences/random_genomic.fa</td>
  </tr>
</table> 


Output of the benchmarked tools:
<table>
  <tr>
    <th>Tool</th>
    <th>Folder</th>
  </tr>
  <tr>
    <td>CNCI</td>
    <td>Supplement/Output/CNCI</td>
  </tr>
  <tr>
    <td>CPAT</td>
    <td>Supplement/Output/CPAT</td>
  </tr>
  <tr>
     <td>CPC2</td>
    <td>Supplement/Output/CPC2</td>
  </tr>
  <tr>
     <td>PLEK</td>
    <td>Supplement/Output/PLEK</td>
  </tr>
  <tr>
     <td>FEELnc</td>
    <td>Supplement/Output/FEELnc</td>
  </tr>
</table>

Our summary of the results can be found as plain text in Supplement/Results/results.txt.
<br><br>
Data used in cite score ranking (last updated: 01.12.21) can be found als .xlsx table and PDF under Supplement/Citations.