rewire.it
Dataset subset

Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)

Dataset subset reported in SegmentNT supplementary information: complete Tables 2 and 3. Exact split manifest remains unextracted; source-table identity is retained.

Evaluation results

21 evaluations · 42 metric rows. Different protocols are not a single leaderboard.

Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: BPNet arch. largeProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.21 (± 0.001) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.001

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

BPNet arch. large on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 2; model BPNet arch. large; column splice acceptor
Configuration: BPNet arch. largeProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.22 (± 0.003) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.003

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

BPNet arch. large on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 2; model BPNet arch. large; column splice acceptor
Configuration: BPNet arch.Protocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.02 (± 0.000) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.000

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

BPNet arch. on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 1; model BPNet arch.; column splice acceptor
Configuration: BPNet arch.Protocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.03 (± 0.004) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.004

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

BPNet arch. on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 1; model BPNet arch.; column splice acceptor
Configuration: Random-Init (only head)Protocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.00 (± 0.000) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.000

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

Random-Init (only head) on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 9; model Random-Init (only head); column splice acceptor
Configuration: Random-Init (only head)Protocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.00 (± 0.001) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.001

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

Random-Init (only head) on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 9; model Random-Init (only head); column splice acceptor
Configuration: Random-InitProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.06 (± 0.002) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

Random-Init on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 10; model Random-Init; column splice acceptor
Configuration: Random-InitProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.09 (± 0.003) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.003

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

Random-Init on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 10; model Random-Init; column splice acceptor
Configuration: SegmentBorzoi-30kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.10 (± 0.002) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentBorzoi-30kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 20; model SegmentBorzoi-30kb; column splice acceptor
Configuration: SegmentBorzoi-30kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.00 (± 0.012) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.012

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentBorzoi-30kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 20; model SegmentBorzoi-30kb; column splice acceptor
Configuration: SegmentBorzoi-524kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.08 (± 0.032) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.032

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentBorzoi-524kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 21; model SegmentBorzoi-524kb; column splice acceptor
Configuration: SegmentBorzoi-524kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.04 (± 0.046) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.046

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentBorzoi-524kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 21; model SegmentBorzoi-524kb; column splice acceptor
Configuration: SegmentEnformer-196kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.02 (± 0.001) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.001

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentEnformer-196kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 19; model SegmentEnformer-196kb; column splice acceptor
Configuration: SegmentEnformer-196kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.00 (± 0.000) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.000

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentEnformer-196kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 19; model SegmentEnformer-196kb; column splice acceptor
Configuration: SegmentEnformer-30kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.01 (± 0.000) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.000

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentEnformer-30kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 18; model SegmentEnformer-30kb; column splice acceptor
Configuration: SegmentEnformer-30kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.00 (± 0.000) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.000

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentEnformer-30kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 18; model SegmentEnformer-30kb; column splice acceptor
Configuration: SegmentNT-10kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.65 (± 0.006) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.006

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-10kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 15; model SegmentNT-10kb; column splice acceptor
Configuration: SegmentNT-10kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.71 (± 0.006) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.006

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-10kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 15; model SegmentNT-10kb; column splice acceptor
Configuration: SegmentNT-20kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.64 (± 0.003) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.003

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-20kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 16; model SegmentNT-20kb; column splice acceptor
Configuration: SegmentNT-20kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.71 (± 0.003) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.003

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-20kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 16; model SegmentNT-20kb; column splice acceptor
Configuration: SegmentNT-30kbProtocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.65 (± 0.002) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-30kb on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 17; model SegmentNT-30kb; column splice acceptor
Configuration: SegmentNT-30kbProtocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.73 (± 0.002) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-30kb on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 17; model SegmentNT-30kb; column splice acceptor
Configuration: SegmentNT-3kb (NTv1 human; 2.5B)Protocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.57 (± 0.002) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-3kb (NTv1 human; 2.5B) on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 12; model SegmentNT-3kb (NTv1 human; 2.5B); column splice acceptor
Configuration: SegmentNT-3kb (NTv1 human; 2.5B)Protocol: SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.62 (± 0.002) mcc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.002

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-3kb (NTv1 human; 2.5B) on SegmentNT human genome annotation splice acceptor MCC: splice acceptor: per-nucleotide annotation (MCC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 2; PDF page 4 (printed 3); block 2; data row 12; model SegmentNT-3kb (NTv1 human; 2.5B); column splice acceptor
Configuration: SegmentNT-3kb (only head)Protocol: SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)
Dataset subset: Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
0.58 (± 0.004) auprc
dimensionless · higher

Uncertainty: type: standard_deviation; value: 0.004

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · source checked
Methods, coverage and source

SegmentNT-3kb (only head) on SegmentNT human genome annotation splice acceptor auPRC: splice acceptor: per-nucleotide annotation (auPRC)

Test chromosomes 20 and 21; validation chromosome 22; training remaining chromosomes. Test chunks with genes homologous to train/validation genes excluded using Ensembl BioMart accessed 2024-05-08; homologous distal regulatory elements not excluded. Ten test-set samplings with sliding windows beginning at different genomic starting positions. Mean plus reported standard deviation; not ten training seeds. Best validation checkpoint by average MCC across 14 elements. Per-nucleotide predictions pooled across test sequences separately for each genomic element. MCC and auPRC are separate metrics, not cross-element or cross-table pooled comparisons.

Aggregation: Not reported

SegmentNT supplementary information: complete Tables 2 and 3 · Supplementary Table 3; PDF page 5 (printed 4); block 2; data row 11; model SegmentNT-3kb (only head); column splice acceptor

Source checking is not independent reproduction. Release 2026-09-23-2b89723c6dd9.

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2 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-09-23-2b89723c6dd9
Property and statementOriginal source and locationReview and provenance
description
Dataset subset reported in SegmentNT supplementary information: complete Tables 2 and 3. Exact split manifest remains unextracted; source-table identity is retained.
Context-only references
SegmentNT supplementary information: complete Tables 2 and 3

Original source ↗

No field-specific location recorded

Version: Published supplementary information to s41592-025-02881-2; SHA-256 pinned snapshot
Retrieved: 2026-09-23T11:23:43.985410+00:00

not individually reviewed

No individual claim review recorded

Audit details

Field: description

Source artifact SHA-256: c4ad23a62ab161a464fe789e5dd167cf2bfe9f43a91a9c3fb1261b99a5594b0f

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

name
Human genome splice acceptor test chromosomes 20 and 21 (SegmentNT human genome annotation split)
Context-only references
SegmentNT supplementary information: complete Tables 2 and 3

Original source ↗

No field-specific location recorded

Version: Published supplementary information to s41592-025-02881-2; SHA-256 pinned snapshot
Retrieved: 2026-09-23T11:23:43.985410+00:00

not individually reviewed

No individual claim review recorded

Audit details

Field: name

Source artifact SHA-256: c4ad23a62ab161a464fe789e5dd167cf2bfe9f43a91a9c3fb1261b99a5594b0f

Hash scope: Hash scope not separately documented; inspect source record

Inspected artifact

Sources and history

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Release 2026-09-23-2b89723c6dd9 · Record review: source checked

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Technical metadata and extraction receipts

Stable ID: segmentnt-supplement-2025-dataset-human-genome-splice-acceptor-test-chromosomes-20-and-21

areas
genomics
missing metadata
version: unreported; url: unextracted
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