Transform lengthy academic papers into concise, structured 250-word abstracts.
中文简介正在准备中。当前显示原文说明。
Use Biopython to read/write/convert biological sequence files (FASTA/GenBank/FASTQ, etc.) and perform basic sequence operations; use when you need reliable sequence I/O, lightweight sequence manipulation, or scalable processing of large sequence datasets.
中文简介正在准备中。当前显示原文说明。
查看安装方法安装前可以查看交给 AI 代理的指令内容。
Bio.Seq.Seq (slicing, reverse complement, transcription/translation).Bio.SeqIO for parsing and writing FASTA/GenBank/FASTQ and other supported formats.SeqIO.index) for large files.biopython>=1.80numpy>=1.21Create config/task_config.json:
{
"input_path": "data/input.fasta",
"input_format": "fasta",
"output_path": "data/output.gb",
"output_format": "genbank",
"min_length": 200,
"max_ambiguous": 0,
"index_db_path": "data/index.sqlite"
}
Run:
python scripts/sequence_io.py
scripts/sequence_io.py (runnable end-to-end):
import json
from pathlib import Path
import numpy as np
from Bio import SeqIO
def gc_fraction(seq: str) -> float:
s = seq.upper()
if not s:
return 0.0
return float((s.count("G") + s.count("C")) / len(s))
def ambiguous_count(seq: str) -> int:
# Treat anything outside A/C/G/T/U as ambiguous for simple filtering.
allowed = set("ACGTU")
return sum(1 for ch in seq.upper() if ch not in allowed)
def main() -> None:
config_path = Path("config/task_config.json")
with config_path.open("r", encoding="utf-8") as f:
cfg = json.load(f)
input_path = Path(cfg["input_path"])
input_format = cfg["input_format"]
output_path = Path(cfg["output_path"])
output_format = cfg["output_format"]
min_length = int(cfg.get("min_length", 0))
max_ambiguous = int(cfg.get("max_ambiguous", 10**9))
output_path.parent.mkdir(parents=True, exist_ok=True)
kept = 0
lengths = []
# Stream records to avoid loading the entire file into memory.
with output_path.open("w", encoding="utf-8") as out_handle:
for record in SeqIO.parse(str(input_path), input_format):
seq_str = str(record.seq)
if len(seq_str) < min_length:
continue
if ambiguous_count(seq_str) > max_ambiguous:
continue
# Example: attach simple stats as annotations (useful for GenBank output).
record.annotations["gc_fraction"] = gc_fraction(seq_str)
SeqIO.write(record, out_handle, output_format)
kept += 1
lengths.append(len(seq_str))
summary = {
"input_path": str(input_path),
"output_path": str(output_path),
"kept_records": kept,
"length_min": int(np.min(lengths)) if lengths else 0,
"length_max": int(np.max(lengths)) if lengths else 0,
"length_mean": float(np.mean(lengths)) if lengths else 0.0,
}
Path("config").mkdir(parents=True, exist_ok=True)
with Path("config/summary.json").open("w", encoding="utf-8") as f:
json.dump(summary, f, ensure_ascii=False, indent=2)
if __name__ == "__main__":
main()
Configuration convention
config/task_config.json as an intermediate artifact.python scripts/<task_name>.py.-- parameters; prefer config files for reproducibility.encoding="utf-8". JSON output must use ensure_ascii=False.Parsing and writing
SeqIO.parse(path, format) for streaming iteration over records.SeqIO.write(records_or_record, handle, format) to serialize records.Large-file strategies
SeqIO.index(input_path, format) (creates an on-disk index depending on backend); this avoids loading all sequences into memory.Filtering/statistics
min_length, maximum ambiguous characters, and quality-based criteria for FASTQ.(count(G)+count(C))/length on an uppercased sequence string; handle empty sequences safely.Reference
references/sequence_io.md for additional notes and format-specific behaviors.biopython_sequence_io_result.md unless the skill documentation defines a better convention.Run this minimal verification path before full execution when possible:
No local script validation step is required for this skill.
Expected output format:
Result file: biopython_sequence_io_result.md
Validation summary: PASS/FAIL with brief notes
Assumptions: explicit list if any
还没有评价。欢迎分享你的使用感受。
无需登录即可发表。欢迎分享使用感受、提问,或说明在哪些环境下无法运行。
还没有评论。来写第一条吧。
Transform lengthy academic papers into concise, structured 250-word abstracts.
中文简介正在准备中。当前显示原文说明。
Precision editing tool that reduces abstract word count through intelligent compression techniques, maintaining scientific rigor while meeting strict journal and conference requirements.
中文简介正在准备中。当前显示原文说明。
Refines long medical academic texts into SCI-style unstructured Chinese and English abstracts; use when you need to condense drafts/reports/summaries into bilingual abstracts and generate Summary_Report.md.
中文简介正在准备中。当前显示原文说明。
Generates submission-ready Elsevier/SCI Highlights from manuscript text or extracted PDF/DOCX/TXT content. Use when a user needs 3-5 concise, evidence-grounded highlight bullets for a research paper, review, meta-analysis, case report, or bioinformatics manuscript.
中文简介正在准备中。当前显示原文说明。
Generates complete FAERS pharmacovigilance study designs for multi-drug or class-level safety comparison inside one predefined SOC or AE family using active comparators, disproportionality analysis, subgroup characterization, and reviewer-facing evidence control.
中文简介正在准备中。当前显示原文说明。
Analyze data with `adme-property-predictor` using a reproducible workflow, explicit validation, and structured outputs for review-ready interpretation.
中文简介正在准备中。当前显示原文说明。