Sort the SFT domains table alphabetically

README.md

@@ -334,14 +334,14 @@ order, with no test split, e.g. `load_dataset("HuggingFaceBio/FineDNA", "sft_cha
 
 | config | train | test (in `sft_mix`) | what the rows teach |
 | --- | ---: | ---: | --- |
-| `sft_sequence_continuation` | 58,727 | 27 | predict the next 1–32 nucleotides after a 4–8 kb eukaryotic context |
-| `sft_variant_effect_prediction` | 57,254 | 24 | decide whether a single-nucleotide variant is benign or pathogenic from its sequence window, with templated reasoning |
-| `sft_dna_computation` | 44,925 | 25 | answers computed exactly from the sequence: counting, GC content, melting temperature, translation, restriction sites, base lookup, coordinates, edits, rewriting |
-| `sft_sequence_classification` | 16,396 | 11 | multiple-choice functional genomics: promoter vs enhancer, species of origin, TF motifs, TF binding sites |
+| `sft_biology_qa` | 4,603 | 3 | genetics, molecular biology and bioinformatics questions from Biology StackExchange, Biostars, real user chats and Nemotron chat data |
 | `sft_chat` | 8,553 | 6 | multi-turn conversations on molecular-biology concepts, the assistant's identity, honesty about its limits, and pushing back on false claims |
-| `sft_sequence_analysis` | 7,561 | 3 | free-text, mostly multi-turn discussion of a pasted sequence: primer checks, annotation, coding potential, troubleshooting |
+| `sft_dna_computation` | 44,925 | 25 | answers computed exactly from the sequence: counting, GC content, melting temperature, translation, restriction sites, base lookup, coordinates, edits, rewriting |
 | `sft_instruction_following` | 5,904 | 1 | answering in the format the user asks for, and following format constraints on biology prompts |
-| `sft_biology_qa` | 4,603 | 3 | genetics, molecular biology and bioinformatics questions from Biology StackExchange, Biostars, real user chats and Nemotron chat data |
+| `sft_sequence_analysis` | 7,561 | 3 | free-text, mostly multi-turn discussion of a pasted sequence: primer checks, annotation, coding potential, troubleshooting |
+| `sft_sequence_classification` | 16,396 | 11 | multiple-choice functional genomics: promoter vs enhancer, species of origin, TF motifs, TF binding sites |
+| `sft_sequence_continuation` | 58,727 | 27 | predict the next 1–32 nucleotides after a 4–8 kb eukaryotic context |
+| `sft_variant_effect_prediction` | 57,254 | 24 | decide whether a single-nucleotide variant is benign or pathogenic from its sequence window, with templated reasoning |
 
 ## RL