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@@ -20,8 +20,8 @@ It takes a samplesheet of BAM/CRAM/FASTQ/FASTA files as input, calculates genome
 4. Run BUSCO ([`busco`](https://busco.ezlab.org/))
 5. Extract BUSCO genes ([`blobtoolkit/extractbuscos`](https://github.com/blobtoolkit/blobtoolkit))
 6. Run Diamond BLASTp against extracted BUSCO genes ([`diamond/blastp`](https://github.com/bbuchfink/diamond))
-7. Run BLASTn against extracted BUSCO genes ([`blast/blastn`](https://www.ncbi.nlm.nih.gov/books/NBK131777/))
-8. Run BLASTx against extracted BUSCO genes ([`blast/blastx`](https://www.ncbi.nlm.nih.gov/books/NBK131777/))
+7. Run BLASTx against sequences with no hit ([`blast/blastn`](https://www.ncbi.nlm.nih.gov/books/NBK131777/))
+8. Run BLASTn against sequences still with not hit ([`blast/blastx`](https://www.ncbi.nlm.nih.gov/books/NBK131777/))
 9. Count BUSCO genes ([`blobtoolkit/countbuscos`](https://github.com/blobtoolkit/blobtoolkit))
 10. Generate combined sequence stats across various window sizes ([`blobtoolkit/windowstats`](https://github.com/blobtoolkit/blobtoolkit))
 11. Imports analysis results into a BlobDir dataset ([`blobtoolkit/blobdir`](https://github.com/blobtoolkit/blobtoolkit))