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README.md
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- biology
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- genomics
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- dna
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configs:
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- config_name: eukaryote_generator
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data_files:
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path: prokaryote_evo2/*.parquet
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---
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# Carbon
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into one Hub dataset with four loadable configs. The goal is to make the
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pretraining mixture reproducible without re-stitching data from multiple upstream
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repositories.
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only useful upstream provenance such as `{"source": "data_mrna_train_chunk1.jsonl.gz"}`
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and, where present, the upstream `record` id.
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| `eukaryote_generator` | [GenerTeam/pretrain_data_eukaryote](https://huggingface.co/datasets/GenerTeam/pretrain_data_eukaryote) | 456 | 376.80 GB | Rich schema with `sequence`, `taxonomy`, `species_type`, `gene_type`, coordinates, and boundary markers. A sampled fungi shard has 187,500 rows with mean sequence length ~1,631 nt. |
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| `mrna_evo2` | [OpenGenome2 mRNA](https://huggingface.co/datasets/arcinstitute/opengenome2/tree/main/json/pretraining_or_both_phases/mrna) | 11 | 54.78 GB | 52,702,454 rows; 115.94 Gbp total; mean 2,200 nt; min 64; max 99,994. |
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| `mrna_splice_evo2` | [OpenGenome2 mRNA splice/promoter](https://huggingface.co/datasets/arcinstitute/opengenome2/tree/main/json/pretraining_or_both_phases/mrna_splice_promoter) | 19 | 92.89 GB | 56,877,762 rows; 197.36 Gbp total; mean 3,470 nt; min 96; max 122,533. |
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| `prokaryote_evo2` | [OpenGenome2 GTDB v220 + IMG/PR](https://huggingface.co/datasets/arcinstitute/opengenome2/tree/main/json/pretraining_or_both_phases/gtdb_v220_imgpr) | 34 | 165.98 GB | 17,408,059 rows; 357.45 Gbp total; mean 20,533 nt; min 20; max 16,040,666. |
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Test splits from opengenome2 are not included (this is a pretraining corpus).
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##
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begin_of_sequence, end_of_sequence, begin_of_gene, end_of_gene, gene_type,
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species_type, strand, sequence, molecule_type, topology, taxonomy, record_id,
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start, end
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```
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```text
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text, metadata
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```
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contains a compact upstream source filename, and for prokaryote rows may also
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include `record`.
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## Usage
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```python
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from datasets import load_dataset
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ds = load_dataset(
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"hf-carbon/carbon-pretraining-corpus",
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"mrna_evo2",
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split="train",
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streaming=True,
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)
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```
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To stream the four configs together:
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```
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specific training mixture.
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- `json/pretraining_or_both_phases/mrna/*_train_*.jsonl.gz`
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- `json/pretraining_or_both_phases/mrna_splice_promoter/*_train_*.jsonl.gz`
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- `json/pretraining_or_both_phases/gtdb_v220_imgpr/*_train_*.jsonl.gz`
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##
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- OpenGenome2 test chunks are intentionally omitted.
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- No additional deduplication or quality filtering was applied beyond upstream processing.
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- The configs are schema-asymmetric: `eukaryote_generator` has a rich structured schema, while OpenGenome2-derived configs are `text` plus `metadata`.
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- Sequence casing, ambiguity codes, and length distributions differ by upstream source.
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@misc{generteam2025generator,
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title = {GENERATOR: A Long-Context Generative Genomic Foundation Model},
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author = {GenerTeam},
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year = {2025},
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eprint = {2502.07272},
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archivePrefix= {arXiv},
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}
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```
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- biology
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- genomics
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- dna
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pretty_name: Carbon Pretraining Corpus
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size_categories:
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- 1T<n<10T
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language: []
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configs:
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- config_name: eukaryote_generator
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data_files:
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path: prokaryote_evo2/*.parquet
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---
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# 𧬠Carbon Pretraining Corpus
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> **~127M DNA & RNA sequences Β· 1 trillion nucleotides** β the DNA pretraining mixture used to train [Carbon](https://github.com/hf-carbon/carbon), a genomic foundation model.
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This dataset is a collection of data sources intended for training genomic foundation models, such as Carbon. It contains DNA and RNA sequences spanning eukaryote and prokaryote species, spanning fungi, plants, animals, bacteria...
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And has almost 1T DNA base pairs (160B tokens with Carbon's 6-mer tokenizer).
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| Subset | Domain | Source | Size | Rows | Nucleotides |
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| `eukaryote_generator` | Eukaryote genomes | GenerTeam / GENERATOR | 376.8 GB | 48.02 M | ~420 Gbp |
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| `mrna_evo2` | Messenger RNA | Arc Institute / OpenGenome2 | 54.8 GB | 52,702,454 | ~115.9 Gbp |
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| `mrna_splice_evo2` | mRNA + splice & promoter | Arc Institute / OpenGenome2 | 92.9 GB | 56,877,762 | ~197.4 Gbp |
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| `prokaryote_evo2` | Prokaryote genomes (GTDB + IMG/PR) | Arc Institute / OpenGenome2 | 166.0 GB | 17,408,059 | ~357.5 Gbp |
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> βΉοΈ Nucleotides are counted in **base pairs (Gbp = billion nucleotides)**. The prokaryote subset has the longest individual sequences (mean ~20 K nt; max ~16 M nt) because it contains whole chromosomal chunks.
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## What is this?
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**Quick biology primer**
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DNA is the molecule that stores genetic information in all living things. It is a sequence of four letters β **A, T, G, C** β and a genome can be anywhere from thousands to billions of these letters long. Training a language model on DNA means treating those letters like tokens and learning the statistical patterns of life.
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This corpus covers three major layers of biological complexity:
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- **Eukaryotes** β organisms with a nucleus (animals, plants, fungi, protists). Complex, large genomes with introns, regulatory regions, and lots of repetition.
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- **Prokaryotes** β bacteria and archaea. Simpler, denser genomes; genes are packed tightly with less non-coding "junk."
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- **mRNA** β the processed, spliced transcript of a gene. This is what actually gets translated into protein. Much shorter than full genomic sequences. Including mRNA teaches the model about gene structure without the noise of intergenic regions.
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## Loading the data
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```python
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from datasets import load_dataset
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ds = load_dataset(
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"hf-carbon/carbon-pretraining-corpus",
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"mrna_evo2", # or: eukaryote_generator | mrna_splice_evo2 | prokaryote_evo2
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split="train",
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streaming=True,
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)
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for example in ds.take(3):
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print(example)
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```
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## Subset Details
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### 1. `eukaryote_generator` β Eukaryote Genomes
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**Source:** [GenerTeam/pretrain_data_eukaryote](https://huggingface.co/datasets/GenerTeam/pretrain_data_eukaryote) Β· MIT License
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**What it contains:** Genomic sequences from eukaryotic organisms (fungi, plants, animals, and more), packaged by the GenerTeam as part of their [GENERATOR](https://arxiv.org/abs/2502.07272) genomic foundation model. This is the main part is Carbon training data, which is focused on Eukaryote species. Each row carries full taxonomic metadata, gene type, strand orientation, and chromosome coordinates alongside the raw sequence.
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We filter out sequences longer than 100 kbp, as excluding them improves training performance on DNA donwstream benchmarks. For long-context training, you can concatenate genes from the same contig to build longer samples.
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**Schema:**
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```
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begin_of_sequence bool β special boundary marker
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end_of_sequence bool β special boundary marker
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begin_of_gene bool β marks gene start
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end_of_gene bool β marks gene end
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gene_type str β e.g. "protein_coding", "ncRNA", "pseudogene"
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species_type str β e.g. "fungi", "plant", "vertebrate"
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strand str β "+" or "-" (which DNA strand)
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sequence str β the raw nucleotide string (A/T/G/C/N...)
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molecule_type str β e.g. "genomic DNA"
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topology str β "linear" or "circular"
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taxonomy str β full NCBI taxonomy lineage
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record_id str β upstream GenBank/RefSeq accession
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start int β coordinate start on chromosome
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end int β coordinate end on chromosome
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```
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**Example row (sequence truncated):**
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```json
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{
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"species_type": "fungi",
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"gene_type": "protein_coding",
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"strand": "+",
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"sequence": "ATGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGCTAGC...",
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"taxonomy": "Eukaryota; Fungi; Ascomycota; ...",
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"record_id": "NC_001224.1",
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"start": 1872,
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"end": 3503
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}
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```
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### 2. `mrna_evo2` β Messenger RNA Sequences
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**Source:** [arcinstitute/opengenome2](https://huggingface.co/datasets/arcinstitute/opengenome2) Β· Apache-2.0 License Β· `mrna` split
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**What it contains:** Processed mRNA sequences β the "final edited" version of a gene after the cell has removed introns (non-coding interruptions) and kept only the exons. This is the sequence that gets read to produce protein. These sequences are shorter and more information-dense than raw genomic DNA.
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**Schema:**
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```
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text str β the raw nucleotide sequence
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metadata dict β {"source": "data_mrna_train_chunk1.jsonl.gz", "record": "..."}
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```
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**Stats:** 52.7 M rows Β· mean 2,200 nt Β· min 64 nt Β· max ~100 K nt Β· 115.9 Gbp total
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### 3. `mrna_splice_evo2` β Augmented mRNA Transcripts
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**Source:** [arcinstitute/opengenome2](https://huggingface.co/datasets/arcinstitute/opengenome2) Β· Apache-2.0 Β· `mrna_splice_promoter` split
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**What it contains:** The same mRNA transcripts as `mrna_evo2`, with augmentations applied by the Evo2 team: each transcript gets an extra 1,024 bp of upstream promoter sequence prepended, and an extra 32 bp of flanking sequence around each exon boundary to expose splice sites. The resulting exon chunks are concatenated with a special `@` separator into a single stitched sequence per transcript.
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Sequences here are systematically longer than `mrna_evo2` β the extra promoter and splice flanks are the only difference, not a different set of genes.
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**Stats:** 56.9 M rows Β· mean 3,470 nt Β· min 96 nt Β· max ~122 K nt Β· 197.4 Gbp total
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### 4. `prokaryote_evo2` β Prokaryote Genomes (Bacteria & Archaea)
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**Upstream:** [arcinstitute/opengenome2](https://huggingface.co/datasets/arcinstitute/opengenome2) Β· Apache-2.0 License Β· `gtdb_v220_imgpr` split
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**What it contains:** Long chromosomal chunks from bacteria and archaea, sourced from [GTDB v220](https://gtdb.ecogenomic.org/) (a curated taxonomy of ~85 K prokaryote genomes) and [IMG/PR](https://img.jgi.doe.gov/) (a DOE database of environmental prokaryote sequences). Prokaryote genomes are compact β genes sit back-to-back with minimal intergenic space β so these sequences are biologically rich per nucleotide.
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**Schema:** identical to the mRNA subsets
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```
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text str β nucleotide sequence (can be megabases long)
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metadata dict β {"source": "gtdb_..._train_chunk1.jsonl.gz", "record": "GCF_..."}
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```
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**Stats:** 17.4 M rows Β· mean 20,533 nt Β· min 20 nt Β· **max ~16 M nt** Β· 357.5 Gbp total
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## βοΈ Carbon Training Mixture
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The proportions below reflect the target mixture for Carbon's pure-DNA pretraining runs (1 T token target):
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| Subset | Approx. weight |
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| `prokaryote_evo2` | ~70% |
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| `mrna_splice_evo2` | ~15% |
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| `mrna_evo2` | ~10% |
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| `eukaryote_generator` | ~5% |
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### Metadata conditioning in Carnon training (`eukaryote_generator` only)
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In Carbon we added optional metadata tags to a fraction of eukaryote sequences, so the model learns to use biological context when available but doesn't depend on it. Tags are prepended before the sequence with random dropout at tokenization time:
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```text
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# 50% of sequences β no tags
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<dna>ATGCTAGCTA...</dna>
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# 16.7% β species + gene type
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<species>fungi<gene_type>protein_coding<dna>ATGCTAGCTA...</dna>
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# 16.7% β species only
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<species>fungi<dna>ATGCTAGCTA...</dna>
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# 16.7% β gene type only
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<gene_type>protein_coding<dna>ATGCTAGCTA...</dna>
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```
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At inference time you can prompt with any combination of tags or none at all. The three OpenGenome2 subsets are tokenized as plain `<dna>SEQUENCE</dna>` without metadata conditioning.
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