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README.md CHANGED
@@ -11,14 +11,22 @@ tags:
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  - benchmark
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  - parquet
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  configs:
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- - config_name: default
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  data_files:
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  - split: train
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- path: train.parquet
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  - split: validation
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- path: validation.parquet
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  - split: test
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- path: test.parquet
 
 
 
 
 
 
 
 
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  ---
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  # GLM-Tang Task 5: INSERT-seq RNA Output
@@ -32,13 +40,13 @@ embryonic stem cells.
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  ```python
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  from datasets import load_dataset
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- dataset = load_dataset("Taykhoom/insert-seq-glm-tang")
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  train = dataset["train"]
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  validation = dataset["validation"]
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  test = dataset["test"]
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  ```
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- ## Dataset size
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  | Split | Rows |
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  |---|---:|
@@ -78,10 +86,10 @@ HDF5 target columns:
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  The released model does **not** train on raw total RNA. It uses:
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  ```python
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- label = log1p(totalRNA_average)
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  ```
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- This transformed value is the model-facing `label`.
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  The raw and auxiliary assay values are retained as:
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@@ -95,16 +103,17 @@ These are targets/measurements, not sequence features.
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  | Column | Description |
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  |---|---|
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- | `split` | Released `train`, `val`, or `test` partition. |
 
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  | `sequence` | Exact 173 nt archived model input in transcribed orientation. |
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- | `label` | `log1p(totalRNA_average)`, matching released training/evaluation code. |
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  | `example_id` | GEO FASTA sequence identifier. |
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  | `source_index` | Zero-based row index in the 16,461-row GEO FASTA/table. |
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  | `raw_total_rna` | Raw `totalRNA_average` assay value. |
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  | `aux_target_run_on_rna` | `runonRNA_average`. |
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  | `aux_target_sort_seq` | `sortseq_average`. |
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  | `source_category`, `source_class`, `source_window`, `source_barcode` | Supplementary Table 2 design provenance. |
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- | `locus_group_id`, `split_leakage` | Source `name` (unique-ID fallback for unnamed rows) and whether that group spans archived partitions. |
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  | `chrom`, `start`, `end`, `strand`, `genome_build` | Nullable source-provided zero-based, half-open GRCm38/mm10 coordinates. |
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  | `coordinates_available` | Whether all four source coordinate fields are present. |
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  | `species` | Always `Mus musculus`. |
@@ -112,14 +121,22 @@ These are targets/measurements, not sequence features.
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  | `is_synthetic` | True only for `randomized_control` rows. |
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  The released code trains with mean-squared error and reports test Pearson
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- correlation and MSE on `label`.
 
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  ## Reproduction boundary
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  The public source has 16,461 rows, while Tang's archive retains 11,417. The
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- source-row selection rule and split seed were not released. This dataset
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- therefore preserves archived row membership/order exactly rather than claiming
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- to recreate that unpublished selection from all GEO rows.
 
 
 
 
 
 
 
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  All archived assay values equal an explicit float32 conversion of the GEO
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  table values.
@@ -131,8 +148,9 @@ the corresponding assay sequence is 173 nt; these values are preserved as
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  source provenance rather than silently adjusted. No hg38 mapping is claimed.
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  The archived split contains 424 `locus_group_id` values in multiple
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- partitions, affecting 848 rows. Group-aware evaluation should use
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- `locus_group_id` and inspect `split_leakage`.
 
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  ## Processing and verification
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  - benchmark
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  - parquet
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  configs:
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+ - config_name: archive
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  data_files:
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  - split: train
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+ path: archive/train.parquet
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  - split: validation
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+ path: archive/validation.parquet
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  - split: test
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+ path: archive/test.parquet
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+ - config_name: corrected
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+ data_files:
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+ - split: train
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+ path: corrected/train.parquet
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+ - split: validation
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+ path: corrected/validation.parquet
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+ - split: test
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+ path: corrected/test.parquet
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  ---
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  # GLM-Tang Task 5: INSERT-seq RNA Output
 
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  ```python
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  from datasets import load_dataset
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+ dataset = load_dataset("Taykhoom/insert-seq-glm-tang", "corrected")
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  train = dataset["train"]
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  validation = dataset["validation"]
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  test = dataset["test"]
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  ```
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+ ## Archive dataset size
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  | Split | Rows |
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  |---|---:|
 
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  The released model does **not** train on raw total RNA. It uses:
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  ```python
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+ label = np.log(totalRNA_average + np.float32(1))
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  ```
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+ This float32 expression is the bit-exact model-facing `label`.
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  The raw and auxiliary assay values are retained as:
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  | Column | Description |
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  |---|---|
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+ | `split` | Selected config's `train`, `val`, or `test` partition. |
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+ | `archive_split` | Original partition; present in `corrected` only. |
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  | `sequence` | Exact 173 nt archived model input in transcribed orientation. |
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+ | `label` | Bit-exact float32 `np.log(totalRNA_average + np.float32(1))`. |
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  | `example_id` | GEO FASTA sequence identifier. |
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  | `source_index` | Zero-based row index in the 16,461-row GEO FASTA/table. |
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  | `raw_total_rna` | Raw `totalRNA_average` assay value. |
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  | `aux_target_run_on_rna` | `runonRNA_average`. |
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  | `aux_target_sort_seq` | `sortseq_average`. |
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  | `source_category`, `source_class`, `source_window`, `source_barcode` | Supplementary Table 2 design provenance. |
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+ | `locus_group_id`, `archive_locus_split_leakage` | Source `name` (unique-ID fallback for unnamed rows) and whether that group spans archive partitions. |
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  | `chrom`, `start`, `end`, `strand`, `genome_build` | Nullable source-provided zero-based, half-open GRCm38/mm10 coordinates. |
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  | `coordinates_available` | Whether all four source coordinate fields are present. |
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  | `species` | Always `Mus musculus`. |
 
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  | `is_synthetic` | True only for `randomized_control` rows. |
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  The released code trains with mean-squared error and reports test Pearson
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+ correlation and MSE on `label`. The previous `log1p` implementation differed
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+ at the bit level for 4,302 rows and is not retained as a duplicate target.
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  ## Reproduction boundary
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  The public source has 16,461 rows, while Tang's archive retains 11,417. The
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+ archive split is deterministic: within each full Supplementary Table 2
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+ `class` in source order, the first `ceil(n/10)` rows are test, the next
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+ `ceil(n/10)` validation, and the remainder train; all `160-333` rows are then
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+ forced to train. Thus all 1,721 retained `160-333` rows are train-only.
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+
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+ The `archive` config preserves those exact rows and splits. The `corrected`
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+ config assigns complete `locus_group_id` groups to a deterministic
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+ class/window-stratified 70/10/20 split. It contains 7,989 train, 1,144
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+ validation, and 2,284 test rows; every class/window stratum with at least three
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+ groups appears in all three splits, and no locus group crosses partitions.
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  All archived assay values equal an explicit float32 conversion of the GEO
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  table values.
 
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  source provenance rather than silently adjusted. No hg38 mapping is claimed.
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  The archived split contains 424 `locus_group_id` values in multiple
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+ partitions, affecting 848 rows. Group-aware evaluation should use the
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+ `corrected` config; `archive_locus_split_leakage` documents the original
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+ contamination.
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  ## Processing and verification
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