lucidrains/enformer-pytorch — Gitpedia

Enformer - Pytorch

Implementation of <a href="https://deepmind.com/blog/article/enformer">Enformer</a>, Deepmind's attention network for predicting gene expression, in Pytorch. This repository also contains the means to fine tune pretrained models for your downstream tasks. The original tensorflow sonnet code can be found <a href="https://github.com/deepmind/deepmind-research/tree/master/enformer">here</a>.

Update: finetuned for predicting pseudobulk chromatin accessibility <a href="https://www.biorxiv.org/content/10.1101/2023.11.27.568764v1">here</a>

Install

bash
$ pip install enformer-pytorch

Usage

python
import torch
from enformer_pytorch import Enformer

model = Enformer.from_hparams(
    dim = 1536,
    depth = 11,
    heads = 8,
    output_heads = dict(human = 5313, mouse = 1643),
    target_length = 896,
)
    
seq = torch.randint(0, 5, (1, 196_608)) # for ACGTN, in that order (-1 for padding)
output = model(seq)

output['human'] # (1, 896, 5313)
output['mouse'] # (1, 896, 1643)

You can also directly pass in the sequence as one-hot encodings, which must be float values

python
import torch
from enformer_pytorch import Enformer, seq_indices_to_one_hot

model = Enformer.from_hparams(
    dim = 1536,
    depth = 11,
    heads = 8,
    output_heads = dict(human = 5313, mouse = 1643),
    target_length = 896,
)

seq = torch.randint(0, 5, (1, 196_608))
one_hot = seq_indices_to_one_hot(seq)

output = model(one_hot)

output['human'] # (1, 896, 5313)
output['mouse'] # (1, 896, 1643)

Finally, one can fetch the embeddings, for fine-tuning and otherwise, by setting the return_embeddings flag to be True on forward

python
import torch
from enformer_pytorch import Enformer, seq_indices_to_one_hot

model = Enformer.from_hparams(
    dim = 1536,
    depth = 11,
    heads = 8,
    output_heads = dict(human = 5313, mouse = 1643),
    target_length = 896,
)

seq = torch.randint(0, 5, (1, 196_608))
one_hot = seq_indices_to_one_hot(seq)

output, embeddings = model(one_hot, return_embeddings = True)

embeddings # (1, 896, 3072)

For training, you can directly pass the head and target in to get the poisson loss

python
import torch
from enformer_pytorch import Enformer, seq_indices_to_one_hot

model = Enformer.from_hparams(
    dim = 1536,
    depth = 11,
    heads = 8,
    output_heads = dict(human = 5313, mouse = 1643),
    target_length = 200,
).cuda()

seq = torch.randint(0, 5, (196_608 // 2,)).cuda()
target = torch.randn(200, 5313).cuda()

loss = model(
    seq,
    head = 'human',
    target = target
)

loss.backward()

# after much training

corr_coef = model(
    seq,
    head = 'human',
    target = target,
    return_corr_coef = True
)

corr_coef # pearson R, used as a metric in the paper

Pretrained Model

Deepmind has released the weights for their tensorflow sonnet Enformer model! I have ported it over to Pytorch and uploaded it to <a href="https://huggingface.co/EleutherAI/enformer-official-rough">🤗 Huggingface</a> (~1GB). There are still some rounding errors that seem to be accruing across the layers, resulting in an absolute error as high as 0.5. However, correlation coefficient look good so I am releasing the 'rough'ly working version. Will keep working on figuring out where the numerical errors are happening (it may be the attention pooling module, as I noticed the attention logits are pretty high).

Update: <a href="https://github.com/jstjohn">John St. John</a> did some work and found that the enformer-official-rough model hits the reported marks in the paper - human pearson R of 0.625 for validation, and 0.65 for test.

Update: As of version 0.8.0, if one were to use the from_pretrained function to load the pretrained model, it should automatically use precomputed gamma positions to address a difference between tensorflow and pytorch xlogy. This should resolve the numerical discrepancy above. If you were to further finetune and not be using the from_pretrained function, please make sure to set use_tf_gamma = True when using .from_hparams to instantiate the Enformer

bash
$ pip install enformer-pytorch>=0.5

Loading the model

python
from enformer_pytorch import from_pretrained

enformer = from_pretrained('EleutherAI/enformer-official-rough')

Quick sanity check on a single human validation point

python
$ python test_pretrained.py
# 0.5963 correlation coefficient on a validation sample

This is all made possible thanks to HuggingFace's custom model feature.

You can also load, with overriding of the target_length parameter, if you are working with shorter sequence lengths

python
from enformer_pytorch import from_pretrained

model = from_pretrained('EleutherAI/enformer-official-rough', target_length = 128, dropout_rate = 0.1)

# do your fine-tuning

To save on memory during fine-tuning a large Enformer model

python
from enformer_pytorch import from_pretrained

enformer = from_pretrained('EleutherAI/enformer-official-rough', use_checkpointing = True)

# finetune enformer on a limited budget

Fine-tuning

This repository will also allow for easy fine-tuning of Enformer.

Fine-tuning on new tracks

python
import torch
from enformer_pytorch import from_pretrained
from enformer_pytorch.finetune import HeadAdapterWrapper

enformer = from_pretrained('EleutherAI/enformer-official-rough')

model = HeadAdapterWrapper(
    enformer = enformer,
    num_tracks = 128,
    post_transformer_embed = False   # by default, embeddings are taken from after the final pointwise block w/ conv -> gelu - but if you'd like the embeddings right after the transformer block with a learned layernorm, set this to True
).cuda()

seq = torch.randint(0, 5, (1, 196_608 // 2,)).cuda()
target = torch.randn(1, 200, 128).cuda()  # 128 tracks

loss = model(seq, target = target)
loss.backward()

Finetuning on contextual data (cell type, transcription factor, etc)

python
import torch
from enformer_pytorch import from_pretrained
from enformer_pytorch.finetune import ContextAdapterWrapper

enformer = from_pretrained('EleutherAI/enformer-official-rough')
    
model = ContextAdapterWrapper(
    enformer = enformer,
    context_dim = 1024
).cuda()

seq = torch.randint(0, 5, (1, 196_608 // 2,)).cuda()

target = torch.randn(1, 200, 4).cuda()  # 4 tracks
context = torch.randn(4, 1024).cuda()   # 4 contexts for the different 'tracks'

loss = model(
    seq,
    context = context,
    target = target
)

loss.backward()

Finally, there is also a way to use attention aggregation from a set of context embeddings (or a single context embedding). Simply use the ContextAttentionAdapterWrapper

python
import torch
from enformer_pytorch import from_pretrained
from enformer_pytorch.finetune import ContextAttentionAdapterWrapper

enformer = from_pretrained('EleutherAI/enformer-official-rough')
    
model = ContextAttentionAdapterWrapper(
    enformer = enformer,
    context_dim = 1024,
    heads = 8,              # number of heads in the cross attention
    dim_head = 64           # dimension per head
).cuda()

seq = torch.randint(0, 5, (1, 196_608 // 2,)).cuda()

target = torch.randn(1, 200, 4).cuda()      # 4 tracks
context = torch.randn(4, 16, 1024).cuda()   # 4 contexts for the different 'tracks', each with 16 tokens

context_mask = torch.ones(4, 16).bool().cuda() # optional context mask, in example, include all context tokens

loss = model(
    seq,
    context = context,
    context_mask = context_mask,
    target = target
)

loss.backward()

Data

You can use the GenomicIntervalDataset to easily fetch sequences of any length from a <a href="https://genome.ucsc.edu/FAQ/FAQformat.html#format1">.bed</a> file, with greater context length dynamically computed if specified

python
import torch
import polars as pl
from enformer_pytorch import Enformer, GenomeIntervalDataset

filter_train = lambda df: df.filter(pl.col('column_4') == 'train')

ds = GenomeIntervalDataset(
    bed_file = './sequences.bed',                       # bed file - columns 0, 1, 2 must be <chromosome>, <start position>, <end position>
    fasta_file = './hg38.ml.fa',                        # path to fasta file
    filter_df_fn = filter_train,                        # filter dataframe function
    return_seq_indices = True,                          # return nucleotide indices (ACGTN) or one hot encodings
    shift_augs = (-2, 2),                               # random shift augmentations from -2 to +2 basepairs
    context_length = 196_608,
    # this can be longer than the interval designated in the .bed file,
    # in which case it will take care of lengthening the interval on either sides
    # as well as proper padding if at the end of the chromosomes
    chr_bed_to_fasta_map = {
        'chr1': 'chromosome1',  # if the chromosome name in the .bed file is different than the key name in the fasta file, you can rename them on the fly
        'chr2': 'chromosome2',
        'chr3': 'chromosome3',
        # etc etc
    }
)

model = Enformer.from_hparams(
    dim = 1536,
    depth = 11,
    heads = 8,
    output_heads = dict(human = 5313, mouse = 1643),
    target_length = 896,
)

seq = ds[0] # (196608,)
pred = model(seq, head = 'human') # (896, 5313)

To return the random shift value, as well as whether reverse complement was activated (in the case you need to reverse the corresponding chip-seq target data), just set return_augs = True when initializing the GenomicIntervalDataset

python
import torch
import polars as pl
from enformer_pytorch import Enformer, GenomeIntervalDataset

filter_train = lambda df: df.filter(pl.col('column_4') == 'train')

ds = GenomeIntervalDataset(
    bed_file = './sequences.bed',                       # bed file - columns 0, 1, 2 must be <chromosome>, <start position>, <end position>
    fasta_file = './hg38.ml.fa',                        # path to fasta file
    filter_df_fn = filter_train,                        # filter dataframe function
    return_seq_indices = True,                          # return nucleotide indices (ACGTN) or one hot encodings
    shift_augs = (-2, 2),                               # random shift augmentations from -2 to +2 basepairs
    rc_aug = True,                                      # use reverse complement augmentation with 50% probability
    context_length = 196_608,
    return_augs = True                                  # return the augmentation meta data
)

seq, rand_shift_val, rc_bool = ds[0] # (196608,), (1,), (1,)

Appreciation

Special thanks goes out to <a href="https://www.eleuther.ai/">EleutherAI</a> for providing the resources to retrain the model, during a time when the official model from Deepmind had not been released yet.

Thanks also goes out to <a href="johahi">@johahi</a> for finding out that there are numerical differences between the torch and tensorflow implementations of xlogy. He provided a fix for this difference, which is adopted in this repository in v0.8.0

Todo

Citations

bibtex
@article {Avsec2021.04.07.438649,
    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},
    elocation-id = {2021.04.07.438649},
    year    = {2021},
    doi     = {10.1101/2021.04.07.438649},
    publisher = {Cold Spring Harbor Laboratory},
    URL     = {https://www.biorxiv.org/content/early/2021/04/08/2021.04.07.438649},
    eprint  = {https://www.biorxiv.org/content/early/2021/04/08/2021.04.07.438649.full.pdf},
    journal = {bioRxiv}
}

bibtex
@misc{liu2022convnet,
    title   = {A ConvNet for the 2020s},
    author  = {Zhuang Liu and Hanzi Mao and Chao-Yuan Wu and Christoph Feichtenhofer and Trevor Darrell and Saining Xie},
    year    = {2022},
    eprint  = {2201.03545},
    archivePrefix = {arXiv},
    primaryClass = {cs.CV}
}