Dataset
BEACON:Isoform
BEACON:Isoform
Not in the Core Set 10 of the 93 cleared all five gates
- Task
- Regression, RNA Processing Prediction
- Level
- RNA
- Species
- Homo sapiens
- Sequences
- 228,388 across 3 splits
- Sequence length
- 186 to 186
- Licence
- Apache-2.0
Read the 5 full reports for this dataset Every distribution, probe fit and overlapping sequence behind the numbers below
-
Fail
worst flag across the ten checks on
train, this dataset's reference split - 4 of the ten checks returned Fail on that split 1 returned Warning, 0 could not be scored
- 0.749 AUROC from the strongest single sequence feature, which is Per sequence nucleotide content A lower bound on what a model could recover from the sequences alone
- 37.24% of one split's sequences were also present in another, at worst The largest of 2 split comparisons: train vs test
- 0.960 AUROC when all those features are read together rather than one at a time Measured on a held-out split. This is what Core Set membership turns on
Where this sits in the corpus
- Stronger than 70 of the 93 probed datasets
- Higher than 80 of the 92 jointly scored datasets
- More overlap than 84 of the 92 scanned datasets
A rank among the datasets this run measured, not among benchmarks in general.
What the checks returned
Worst flag across the ten checks on the
train split: Fail
Of the nine checks that measure a single split,
9 ran on train and
9 were scored: 4 returned Fail,
1 returned Warning, 0 returned Unknown.
The leakage scan is counted in the flag above but not in these figures,
because it compares pairs of splits rather than measuring one.
Every rollup figure on this page was measured on
train, which is this dataset's reference split
— not a maximum over its splits.
The strongest single feature is Per sequence nucleotide content, which
reaches AUROC 0.749 on the
train split from that feature alone. That is a lower
bound: a stronger feature, or a model, may recover more.
The leakage scan found that 37.24% of the sequences
in test were also present in
train; the same comparison the other way puts
29.89% of train in test.
That is the largest of the two split comparisons the scan
made here.
What each of the ten checks measures · What a flag is, and what it does not say · Why one split is quoted
The reports behind those flags
The full report genomic-benchmarks-qc rendered for each split and
each split pair, with every distribution, every probe fit, and every
individually-listed overlapping sequence behind the numbers on this page. Each
opens inside this site, and the file the tool wrote is one click further on.
- train · seq class distributions
- val · seq class distributions
- test · seq class distributions
- train vs test leakage scan
- train vs val leakage scan
The same features, read together
Every flag above is one feature on its own. This is all of them at once: length, GC, mononucleotide and dinucleotide content and the two per-position profiles, handed to a single model and scored on a held-out split. Nothing is added that the checks do not already look at — the only change is that they are read jointly.
0.960
AUROC from all the checks’ features at once,
measured on the test split
95% interval 0.959 to 0.962, over 49,755 held-out sequences
The strongest single feature reaches 0.749 on its own.
How it was measured, why it exists, and the six datasets it changes the reading of
The nine per-split checks
One row per split, one column per check. The leakage scan is not here because it compares split pairs rather than measuring one split; it has its own section below.
The nine class-distribution checks on each of BEACON:Isoform’s 3 splits. The rollup reports the train row.
Table view
| Split | GC content | Nucleotide content | Dinucleotide content | Sequence lengths | Per position nucleotide | Per position from 3′ | Duplicates within label | Duplicates across labels | Unique bases |
|---|---|---|---|---|---|---|---|---|---|
| train | Warning 0.685 | Fail 0.749 | Fail 0.700 | Pass 0.500 | Fail 0.719 | Fail 0.719 | Pass | Pass | Pass |
| val | Fail 0.705 | Fail 0.757 | Fail 0.703 | Pass 0.500 | Fail 0.708 | Fail 0.708 | Pass | Pass | Pass |
| test | Warning 0.694 | Fail 0.738 | Fail 0.713 | Pass 0.500 | Warning 0.699 | Warning 0.699 | Pass | Pass | Fail |
| Split | Sequence columns | Worst flag | Checks scored | Strongest probe | AUROC | Report |
|---|---|---|---|---|---|---|
train reference |
seq |
Fail | 9 | Per sequence nucleotide content | 0.749 | seq |
val |
seq |
Fail | 9 | Per sequence nucleotide content | 0.757 | seq |
test |
seq |
Fail | 9 | Per sequence nucleotide content | 0.738 | seq |
How far each probe gets
The AUROC each of the six probe checks reaches on each split, from that one feature alone. The axis starts at 0.50 because that is what a feature carrying no class information returns.
What each single-feature probe recovered, on each split. Where a dataset has several sequence columns the strongest is shown; the table view lists every value.
The axis starts at 0.50 because that is what a probe recovering nothing would read. A value is a lower bound: it is what one feature reached, not the most that could be reached.
Table view
| Check | train | val | test |
|---|---|---|---|
| Per sequence GC content | 0.685 | 0.705 | 0.694 |
| Per sequence nucleotide content | 0.749 | 0.757 | 0.738 |
| Per sequence dinucleotide content | 0.700 | 0.703 | 0.713 |
| Sequence lengths | 0.500 | 0.500 | 0.500 |
| Per position nucleotide content | 0.719 | 0.708 | 0.699 |
| Per position reversed nucleotide content | 0.719 | 0.708 | 0.699 |
Split comparisons
For every pair of splits the scan compared, the share of each split whose sequences also appear in the other. Each bar is coloured by the split it counts.
The two directions of a pair are different statements. A held-out split largely contained in train is the one that bears on whether a score on it is a held-out score.
Table view
| Comparison | Share | Flag |
|---|---|---|
| train also in val | 27.44% | Fail |
| val also in train | 36.48% | Fail |
| train also in test | 29.89% | Fail |
| test also in train | 37.24% | Fail |
| Comparison | Flag | Of the first split | Of the second |
|---|---|---|---|
val in train |
Fail | 36.48% | 27.44% |
test in train |
Fail | 37.24% | 29.89% |
Licence, credit, and the data itself
What this data may be used for is its source's decision and not this project's. It is set down here as the curation read it, with the evidence, so that a reader can check the reading rather than take it.
- Licence
- Apache-2.0
- Credit
- 10.1016/j.cell.2019.04.046 — this dataset's
Each split's file, and where it is served from:
train— Isoform_train.csv.gzhuggingface.coval— Isoform_val.csv.gzhuggingface.cotest— Isoform_test.csv.gzhuggingface.co
This licence permits redistribution, so the split files may be republished under its terms rather than only fetched from the links above. The paper states that the datasets and the source code of the benchmark are available at github.com/terry-r123/RNABenchmark, and that repository is Apache-2.0, so the release the authors point at is the licensed one. Recorded with the qualification that the files themselves are served from the Google Drive folder the repository links (19ddrwI8ycvIxkgSV3gDo_VunLofYd4-6), which carries no terms of its own; neither the paper nor its NeurIPS datasheet states a licence for the data separately. Apache-2.0 permits redistribution provided the licence and the attribution notices are kept.
Nearby
- All 3 datasets in BEACON
- All 11 datasets in the task category RNA Processing Prediction
- All 53 datasets on Homo sapiens
Nearest by name in BEACON: BEACON: