The MultiMolecule team has confirmed that the provided model and checkpoints are producing the same intermediate representations as the original implementation.
The team releasing Enformer did not write this model card for this model so this model card has been written by the MultiMolecule team.
Model Details
Enformer is the successor of Basenji. It replaces Basenji's dilated convolution tower with a convolution stem followed by a Transformer trunk, which lets it model long-range genomic interactions. It consumes a long DNA window (~393 kb), passes it through a convolution + attention-pooling stem that downsamples the sequence by
2 ** 7 = 128x
, processes the binned representation with 11 Transformer blocks using Transformer-XL style relative positional encoding, center-crops to 896 output bins, and applies a pointwise head plus a per-species linear track projection with a softplus activation. The prediction is
binned
: the output has shape
(batch_size, target_length, num_tracks)
where each bin summarizes 128 bp of sequence and
num_tracks
is the number of genomic coverage experiments for the selected species.
Model Specification
Input Length
Bin Size
Output Bins
Hidden Size
Layers
Heads
Num Labels
Num Parameters (M)
393216
128
896
1536
11
8
5313
246.2
The default table reports the human output head. The mouse head predicts 1643 tracks.
Developed by
: Žiga Avsec, Vikram Agarwal, Daniel Visentin, Joseph R. Ledsam, Agnieszka Grabska-Barwinska, Kyle R. Taylor, Yannis Assael, John Jumper, Pushmeet Kohli, David R. Kelley
The binned positional axis is treated as the "token" axis: each output position corresponds to one
genomic bin rather than a single nucleotide. The
species
configuration option selects the
human
(5,313 tracks) or
mouse
(1,643 tracks) output head.
Training Details
Enformer was trained to predict genomic coverage tracks (DNase-seq, ATAC-seq, ChIP-seq and CAGE)
from the human and mouse reference genomes.
Training Data
The model was trained on a large compendium of functional genomics experiments aligned to the
human (hg38) and mouse (mm10) reference genomes. The genome was divided into overlapping windows;
for each window the per-128-bp coverage of every experiment served as the regression target.
Training Procedure
The model was trained to minimize a Poisson regression loss between predicted and observed
coverage, using a softplus output activation to keep the predicted coverage non-negative.
Citation
@article{avsec2021effective,
author = {Avsec, {\v{Z}}iga and Agarwal, Vikram and Visentin, Daniel and Ledsam, Joseph R. and Grabska-Barwinska, Agnieszka and Taylor, Kyle R. and Assael, Yannis and Jumper, John and Kohli, Pushmeet and Kelley, David R.},
title = {Effective gene expression prediction from sequence by integrating long-range interactions},
journal = {Nature Methods},
year = 2021,
volume = 18,
number = 10,
pages = {1196--1203},
doi = {10.1038/s41592-021-01252-x},
publisher = {Nature Publishing Group}
}
The artifacts distributed in this repository are part of the MultiMolecule project.
If you use MultiMolecule in your research, you must cite the MultiMolecule project as follows:
@software{chen_2024_12638419,
author = {Chen, Zhiyuan and Zhu, Sophia Y.},
title = {MultiMolecule},
doi = {10.5281/zenodo.12638419},
publisher = {Zenodo},
url = {https://doi.org/10.5281/zenodo.12638419},
year = 2024,
month = may,
day = 4
}
Contact
Please use GitHub issues of
MultiMolecule
for any questions or comments on the model card.
Please contact the authors of the
Enformer paper
for questions or comments on the paper/model.
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