---
tags:
- model_hub_mixin
- pytorch_model_hub_mixin
---

# segment-borzoi

SegmentBorzoi is a segmentation model leveraging [Borzoi](https://www.biorxiv.org/content/10.1101/2023.08.30.555582v1.abstract) to predict the location of several types of genomics 
elements in a sequence at a single nucleotide resolution. It was trained on 14 different classes, including gene (protein-coding genes, lncRNAs, 5’UTR, 3’UTR, exon, intron, splice acceptor and donor sites) and regulatory (polyA signal, tissue-invariant and 
tissue-specific promoters and enhancers, and CTCF-bound sites) elements.


**Developed by:** [InstaDeep](https://huggingface.co/InstaDeepAI)

### How to use

To Be Done



## Training data

The **SegmentBorzoi** model was trained on all human chromosomes except for chromosomes 20 and 21, kept as test set, and chromosome 22, used as a validation set.
During training, sequences are randomly sampled in the genome with associated annotations. However, we keep the sequences in the validation and test set fixed by 
using a sliding window of length 524kb (original borzoi input length) over the chromosomes 20 and 21. The validation set was used to monitor training and for early stopping.

## Training procedure

### Preprocessing

The DNA sequences are tokenized using one-hot encoding similar to the Enformer model

### Architecture

The model is composed of the Borzoi backbone, from which we remove the heads and replaced it by a 1-dimensional U-Net segmentation head made of 2 downsampling convolutional blocks and 2 upsampling convolutional blocks. Each of these 
blocks is made of 2 convolutional layers with 1, 024 and 2, 048 kernels respectively.

### BibTeX entry and citation info

```bibtex
@article{de2024segmentnt,
  title={SegmentNT: annotating the genome at single-nucleotide resolution with DNA foundation models},
  author={de Almeida, Bernardo P and Dalla-Torre, Hugo and Richard, Guillaume and Blum, Christopher and Hexemer, Lorenz and Gelard, Maxence and Pandey, Priyanka and Laurent, Stefan and Laterre, Alexandre and Lang, Maren and others},
  journal={bioRxiv},
  pages={2024--03},
  year={2024},
  publisher={Cold Spring Harbor Laboratory}
}

```