add Rivas dataset

docs/docs/datasets/rivas.md

@@ -0,0 +1,9 @@
+---
+authors:
+  - Zhiyuan Chen
+date: 2024-05-04
+---
+
+# RIVAS
+
+--8<-- "multimolecule/datasets/rivas/README.md:21:"

docs/mkdocs.yml

@@ -19,6 +19,7 @@ nav:
       - RNA:
           - RNAcentral: datasets/rnacentral.md
           - Rfam: datasets/rfam.md
+          - RIVAS: datasets/rivas.md
           - bpRNA-1m: datasets/bprna.md
           - bpRNA-spot: datasets/bprna-spot.md
           - bpRNA-new: datasets/bprna-new.md

multimolecule/datasets/bprna_new/bprna_new.py

@@ -18,6 +18,7 @@
 
 import os
 from collections import namedtuple
+from collections.abc import Mapping
 from pathlib import Path
 
 import torch
@@ -30,20 +31,41 @@
 RNA_SS_data = namedtuple("RNA_SS_data", "seq ss_label length name pairs")
 
 
-def convert_bpseq(bpseq):
-    if isinstance(bpseq, str):
-        bpseq = Path(bpseq)
-    with open(bpseq) as f:
+def convert_bpseq(file) -> Mapping:
+    if not isinstance(file, Path):
+        file = Path(file)
+    with open(file) as f:
         lines = f.read().splitlines()
-    lines = [[int(i) if i.isdigit() else i for i in j.split()] for j in lines]
-    sequence, structure = [], ["."] * len(lines)
-    for row in lines:
-        index, nucleotide, paired_index = row
-        sequence.append(nucleotide)
-        if paired_index > 0 and index < paired_index:
-            structure[index - 1] = "("
-            structure[paired_index - 1] = ")"
-    return {"id": bpseq.stem.split("-")[0], "sequence": "".join(sequence), "secondary_structure": "".join(structure)}
+
+    num_bases = len(lines)
+    sequence = []
+    dot_bracket = ["."] * num_bases
+    pairs = [-1] * num_bases
+
+    for line in lines:
+        parts = line.strip().split()
+        index = int(parts[0]) - 1
+        base = parts[1]
+        paired_index = int(parts[2]) - 1
+
+        sequence.append(base)
+
+        if paired_index >= 0:
+            if paired_index > index:
+                dot_bracket[index] = "("
+                dot_bracket[paired_index] = ")"
+            elif pairs[paired_index] != index:
+                raise ValueError(
+                    f"Inconsistent pairing: Base {index} is paired with {paired_index}, "
+                    f"but {paired_index} is not paired with {index}."
+                )
+            pairs[index] = paired_index
+
+    return {
+        "id": file.stem.split("-")[0],
+        "sequence": "".join(sequence),
+        "secondary_structure": "".join(dot_bracket),
+    }
 
 
 def convert_dataset(convert_config):

multimolecule/datasets/rivas/README.md

@@ -0,0 +1,101 @@
+---
+language: rna
+tags:
+  - Biology
+  - RNA
+license:
+  - agpl-3.0
+size_categories:
+  - 1K<n<10K
+task_categories:
+  - text-generation
+  - fill-mask
+task_ids:
+  - language-modeling
+  - masked-language-modeling
+pretty_name: RIVAS
+library_name: multimolecule
+---
+
+# RIVAS
+
+The RIVAS dataset is a curated collection of RNA sequences and their secondary structures, designed for training and evaluating RNA secondary structure prediction methods.
+The dataset combines sequences from published studies and databases like Rfam, covering diverse RNA families such as tRNA, SRP RNA, and ribozymes.
+The secondary structure data is obtained from experimentally verified structures and consensus structures from Rfam alignments, ensuring high-quality annotations for model training and evaluation.
+
+## Disclaimer
+
+This is an UNOFFICIAL release of the RIVAS dataset by Elena Rivas, et al.
+
+**The team releasing RIVAS did not write this dataset card for this dataset so this dataset card has been written by the MultiMolecule team.**
+
+## Dataset Description
+
+- **Homepage**: https://multimolecule.danling.org/datasets/rivas
+- **Point of Contact**: [Elena Rivas](mailto:[email protected])
+
+## Example Entry
+
+| id                      | sequence                            | secondary_structure                 |
+| ----------------------- | ----------------------------------- | ----------------------------------- |
+| AACY020454584.1_604-676 | ACUGGUUGCGGCCAGUAUAAAUAGUCUUUAAG... | ((((........)))).........((........ |
+
+## Column Description
+
+The converted dataset consists of the following columns, each providing specific information about the RNA secondary structures, consistent with the bpRNA standard:
+
+- **id**:
+    A unique identifier for each RNA entry. This ID is derived from the original `.sta` file name and serves as a reference to the specific RNA structure within the dataset.
+
+- **sequence**:
+    The nucleotide sequence of the RNA molecule, represented using the standard RNA bases:
+
+    - **A**: Adenine
+    - **C**: Cytosine
+    - **G**: Guanine
+    - **U**: Uracil
+
+- **secondary_structure**:
+    The secondary structure of the RNA represented in dot-bracket notation, using up to three types of symbols to indicate base pairing and unpaired regions, as per bpRNA's standard:
+
+    - **Dots (`.`)**: Represent unpaired nucleotides.
+    - **Parentheses (`(` and `)`)**: Represent base pairs in standard stems (page 1).
+    - **Square Brackets (`[` and `]`)**: Represent base pairs in pseudoknots (page 2).
+    - **Curly Braces (`{` and `}`)**: Represent base pairs in additional pseudoknots (page 3).
+
+## Variations
+
+This dataset is available in three variants:
+
+- [RIVAS](https://huggingface.co/datasets/multimolecule/rivas): Includes TrainSetA (3166 sequences) for training, TestSetA (697 sequences) for validation and TestSetB (430 sequences) for testing.
+- [RIVAS-A](https://huggingface.co/datasets/multimolecule/rivas-a): Includes TrainSetA (3166 sequences) and TestSetA (697 sequences), emphasizing sequence diversity while minimizing overlap between training and test sets. Suitable for evaluating RNA secondary structure prediction models on diverse RNA families.
+- [RIVAS-B](https://huggingface.co/datasets/multimolecule/rivas-b): Consists of TrainSetB (1094 sequences) and TestSetB (430 sequences) derived from Rfam alignments, offering additional structural diversity and RNA types not present in RIVAS-A. Designed for testing the generalization capability of models trained on different types of RNA structures.
+
+## Related Datasets
+
+- [bpRNA-spot](https://huggingface.co/datasets/multimolecule/bprna-spot): A subset of RIVAS that applies [CD-HIT (CD-HIT-EST)](https://sites.google.com/view/cd-hit) to remove sequences with more than 80% sequence similarity from RIVAS.
+- [RNAStrAlign](https://huggingface.co/datasets/multimolecule/rnastralign): A database of RNA secondary with the same families as ArchiveII, usually used for training.
+
+## License
+
+This dataset is licensed under the [AGPL-3.0 License](https://www.gnu.org/licenses/agpl-3.0.html).
+
+```spdx
+SPDX-License-Identifier: AGPL-3.0-or-later
+```
+
+## Citation
+
+```bibtex
+@article{rivas2012a,
+  author    = {Rivas, Elena and Lang, Raymond and Eddy, Sean R},
+  journal   = {RNA},
+  month     = feb,
+  number    = 2,
+  pages     = {193--212},
+  publisher = {Cold Spring Harbor Laboratory},
+  title     = {A range of complex probabilistic models for {RNA} secondary structure prediction that includes the nearest-neighbor model and more},
+  volume    = 18,
+  year      = 2012
+}
+```

multimolecule/datasets/rivas/rivas.py

@@ -0,0 +1,60 @@
+# MultiMolecule
+# Copyright (C) 2024-Present  MultiMolecule
+
+# This program is free software: you can redistribute it and/or modify
+# it under the terms of the GNU Affero General Public License as published by
+# the Free Software Foundation, either version 3 of the License, or
+# any later version.
+
+# This program is distributed in the hope that it will be useful,
+# but WITHOUT ANY WARRANTY; without even the implied warranty of
+# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE.  See the
+# GNU Affero General Public License for more details.
+
+# You should have received a copy of the GNU Affero General Public License
+# along with this program.  If not, see <http://www.gnu.org/licenses/>.
+
+from __future__ import annotations
+
+import os
+
+import torch
+from tqdm import tqdm
+
+from multimolecule.datasets.bprna_new.bprna_new import convert_bpseq
+from multimolecule.datasets.conversion_utils import ConvertConfig as ConvertConfig_
+from multimolecule.datasets.conversion_utils import get_files, save_dataset
+
+torch.manual_seed(1016)
+
+
+def _convert_dataset(root):
+    files = get_files(root)
+    return [convert_bpseq(file) for file in tqdm(files, total=len(files))]
+
+
+def convert_dataset(convert_config):
+    root = convert_config.dataset_path
+    train_a = _convert_dataset(os.path.join(root, "TrainSetA"))
+    train_b = _convert_dataset(os.path.join(root, "TrainSetB"))
+    test_a = _convert_dataset(os.path.join(root, "TestSetA"))
+    test_b = _convert_dataset(os.path.join(root, "TestSetB"))
+    output_path, repo_id = convert_config.output_path, convert_config.repo_id
+    save_dataset(convert_config, {"train": train_a, "validation": test_a, "test": test_b})
+    convert_config.output_path = output_path + "-a"
+    convert_config.repo_id = repo_id + "-a"
+    save_dataset(convert_config, {"train": train_a, "test": test_a})
+    convert_config.output_path = output_path + "-b"
+    convert_config.repo_id = repo_id + "-b"
+    save_dataset(convert_config, {"train": train_b, "test": test_b})
+
+
+class ConvertConfig(ConvertConfig_):
+    root: str = os.path.dirname(__file__)
+    output_path: str = os.path.basename(os.path.dirname(__file__))
+
+
+if __name__ == "__main__":
+    config = ConvertConfig()
+    config.parse()  # type: ignore[attr-defined]
+    convert_dataset(config)