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feat: add full 6-step NGS pipeline + fix sequencing WinError 193
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import asyncio
import logging
import os
import platform
import re
import shutil
import tempfile
from typing import Any
import httpx
from app.tools.base import BaseTool
logger = logging.getLogger(__name__)
_IS_WINDOWS = os.name == "nt" or platform.system() == "Windows"
_MINIMAP2_BIN = "minimap2.exe" if _IS_WINDOWS else "minimap2"
BIN_DIR = os.path.join(os.path.dirname(__file__), "..", "bin")
MINIMAP2_PATH = shutil.which("minimap2") or os.path.join(BIN_DIR, _MINIMAP2_BIN)
MINIMAP2_URL = "https://github.com/lh3/minimap2/releases/download/v2.28/minimap2-2.28_x64-linux.tar.bz2"
PIPELINE_TIMEOUT = 600
REFERENCE_URLS = {
"sars-cov-2": "https://hgdownload.soe.ucsc.edu/goldenPath/wuhCor1/bigZips/wuhCor1.fa.gz",
"lambda": "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=nuccore&id=NC_001416&rettype=fasta&retmode=text",
}
SMALL_REFERENCE = "sars-cov-2"
MAX_FASTQ_SIZE = 50 * 1024 * 1024
REF_CACHE_DIR = os.path.join(os.path.dirname(__file__), "..", "data", "references")
def _is_executable(path: str) -> bool:
if not os.path.exists(path):
return False
if _IS_WINDOWS:
return os.path.isfile(path)
return os.access(path, os.X_OK)
async def _ensure_minimap2() -> str:
if _is_executable(MINIMAP2_PATH):
return MINIMAP2_PATH
if _IS_WINDOWS:
logger.warning(
"minimap2 is not available on Windows. "
"Install via: conda install -c bioconda minimap2 OR pip install mappy. "
"Falling back to Python-based read counting."
)
raise FileNotFoundError(
"minimap2 is not available on Windows. "
"Install via: conda install -c bioconda minimap2 OR pip install mappy. "
"Alternatively, run on Linux for full alignment support."
)
dest = MINIMAP2_PATH
os.makedirs(BIN_DIR, exist_ok=True)
logger.info("Downloading minimap2 binary ...")
async with httpx.AsyncClient(timeout=60, follow_redirects=True) as client:
r = await client.get(MINIMAP2_URL)
r.raise_for_status()
import tarfile, io
with tarfile.open(fileobj=io.BytesIO(r.content)) as tar:
for member in tar.getmembers():
if member.name.endswith("minimap2"):
f = tar.extractfile(member)
if f:
with open(dest, "wb") as out:
out.write(f.read())
break
os.chmod(dest, 0o755)
return dest
def _fallback_alignment(fastq_path: str, ref_path: str, sam_path: str) -> dict:
"""Pure-Python fallback when minimap2 is unavailable (e.g. Windows without conda)."""
total = 0
with open(fastq_path) as fin, open(sam_path, "w") as out:
out.write("@HD\tVN:1.6\tSO:unsorted\n")
line_no = 0
qname = ""
seq = ""
qual = ""
for line in fin:
line_no += 1
if line_no % 4 == 1:
qname = line.strip().lstrip("@")
elif line_no % 4 == 2:
seq = line.strip()
elif line_no % 4 == 0:
qual = line.strip()
total += 1
flag = 4 # unmapped
out.write(f"{qname}\t{flag}\t*\t0\t0\t*\t*\t0\t0\t{seq}\t{qual}\n")
return {"mapped_reads": 0, "unmapped_reads": total, "total_alignments": total}
def _generate_synthetic_fastq(ref_seq: str, num_reads: int = 100, read_len: int = 100) -> str:
import random
ref = "".join(line.strip().upper() for line in ref_seq.splitlines() if not line.startswith(">"))
if len(ref) < read_len:
ref = ref * ((read_len // len(ref)) + 1)
lines: list[str] = []
for i in range(num_reads):
start = random.randint(0, len(ref) - read_len)
seq = ref[start:start + read_len]
mut_rate = 0.01
seq = "".join(
random.choice("ACGT") if random.random() < mut_rate else b
for b in seq
)
qual = "".join(chr(33 + min(40, random.randint(20, 40))) for _ in range(read_len))
lines.append(f"@read{i + 1}")
lines.append(seq)
lines.append("+")
lines.append(qual)
return "\n".join(lines)
def _parse_fastq_quality(fastq_path: str) -> dict:
total_reads = 0
total_bases = 0
gc_count = 0
at_count = 0
q_scores: list[int] = []
read_lengths: list[int] = []
seen_seqs: dict[str, int] = {}
line_no = 0
with open(fastq_path) as f:
for line in f:
line_no += 1
if line_no % 4 == 1:
total_reads += 1
elif line_no % 4 == 2:
seq = line.strip()
l = len(seq)
read_lengths.append(l)
total_bases += l
gc_count += seq.count("G") + seq.count("C") + seq.count("g") + seq.count("c")
at_count += seq.count("A") + seq.count("T") + seq.count("a") + seq.count("t")
seen_seqs[seq] = seen_seqs.get(seq, 0) + 1
elif line_no % 4 == 0:
qual = line.strip()
for ch in qual:
q_scores.append(ord(ch) - 33)
if total_reads == 0:
return {"error": "Empty FASTQ file", "total_reads": 0}
mean_q = sum(q_scores) / len(q_scores) if q_scores else 0
min_q = min(q_scores) if q_scores else 0
max_q = max(q_scores) if q_scores else 0
q20 = sum(1 for q in q_scores if q >= 20) / len(q_scores) * 100 if q_scores else 0
q30 = sum(1 for q in q_scores if q >= 30) / len(q_scores) * 100 if q_scores else 0
gc_pct = gc_count / (gc_count + at_count) * 100 if (gc_count + at_count) > 0 else 0
avg_len = sum(read_lengths) / len(read_lengths) if read_lengths else 0
overrepresented = sorted(seen_seqs.items(), key=lambda x: -x[1])[:10]
overrep_pct = [(s, c, c / total_reads * 100) for s, c in overrepresented]
return {
"total_reads": total_reads,
"total_bases": total_bases,
"avg_read_length": round(avg_len, 1),
"min_read_length": min(read_lengths) if read_lengths else 0,
"max_read_length": max(read_lengths) if read_lengths else 0,
"gc_percent": round(gc_pct, 2),
"mean_quality": round(mean_q, 2),
"min_quality": min_q,
"max_quality": max_q,
"q20_percent": round(q20, 2),
"q30_percent": round(q30, 2),
"overrepresented_sequences": [
{"sequence": s[:50], "count": c, "percent": round(p, 2)}
for s, c, p in overrep_pct
],
}
def _parse_sam_for_variants(sam_path: str, reference_seq: str) -> list[dict]:
ref_lines = reference_seq.splitlines()
ref = "".join(line.strip().upper() for line in ref_lines if not line.startswith(">"))
pileup: dict[int, dict[str, int]] = {}
depth_by_pos: dict[int, int] = {}
with open(sam_path) as f:
for line in f:
if line.startswith("@"):
continue
parts = line.strip().split("\t")
if len(parts) < 6:
continue
flag = int(parts[1])
if flag & 4:
continue
pos = int(parts[3])
cigar = parts[5]
seq = parts[9]
genome_pos = pos - 1
ops = re.findall(r"(\d+)([MIDNSHPX=])", cigar)
offset = 0
for length, op in ops:
l = int(length)
if op == "M":
for i in range(l):
p = genome_pos + i
if p < len(ref):
base = seq[offset + i].upper() if offset + i < len(seq) else "N"
if p not in pileup:
pileup[p] = {"A": 0, "C": 0, "G": 0, "T": 0, "N": 0, "del": 0, "ins": 0}
depth_by_pos[p] = depth_by_pos.get(p, 0) + 1
if base in pileup[p]:
pileup[p][base] += 1
else:
pileup[p]["N"] += 1
offset += l
elif op == "I":
offset += l
elif op == "D":
for i in range(l):
p = genome_pos + i
if p not in pileup:
pileup[p] = {"A": 0, "C": 0, "G": 0, "T": 0, "N": 0, "del": 0, "ins": 0}
pileup[p]["del"] += 1
elif op in ("S", "H"):
if op == "S":
offset += l
min_depth = 2
min_alt_freq = 0.2
variants: list[dict] = []
for pos in sorted(pileup.keys()):
counts = pileup[pos]
depth = depth_by_pos.get(pos, sum(counts.values()) - counts.get("del", 0) - counts.get("ins", 0))
if depth < min_depth:
continue
ref_base = ref[pos].upper() if pos < len(ref) else "N"
total = sum(counts.get(b, 0) for b in "ACGTN")
if total == 0:
continue
for base in "ACGT":
if base == ref_base:
continue
alt_count = counts.get(base, 0)
freq = alt_count / total
if freq >= min_alt_freq:
variants.append({
"pos": pos + 1, "ref": ref_base, "alt": base,
"depth": depth, "alt_count": alt_count, "freq": round(freq, 4),
})
variants.sort(key=lambda v: -v["freq"])
return variants[:50]
def _build_consensus(reference_seq: str, variants: list[dict]) -> str:
ref_lines = reference_seq.splitlines()
ref = "".join(line.strip().upper() for line in ref_lines if not line.startswith(">"))
seq = list(ref)
for v in variants:
pos = v.get("pos", 0) - 1
alt = v.get("alt", "")
if 0 <= pos < len(seq):
seq[pos] = alt
return "".join(seq)
def _generate_report(qc: dict, variants: list[dict], ref_name: str) -> dict:
total_variants = len(variants)
snv_count = sum(1 for v in variants if len(v["ref"]) == 1 and len(v["alt"]) == 1)
avg_depth = round(sum(v["depth"] for v in variants) / total_variants, 1) if total_variants else 0
return {
"reference": ref_name,
"qc_summary": {
"total_reads": qc.get("total_reads", 0),
"total_bases": qc.get("total_bases", 0),
"mean_quality": qc.get("mean_quality", 0),
"q30_percent": qc.get("q30_percent", 0),
"gc_percent": qc.get("gc_percent", 0),
},
"variant_summary": {
"total_variants": total_variants,
"snv_count": snv_count,
"avg_depth": avg_depth,
},
"variants": variants,
}
async def _download_fastq(url: str, dest: str) -> str:
async with httpx.AsyncClient(timeout=120, follow_redirects=True) as client:
async with client.stream("GET", url) as r:
r.raise_for_status()
content_length = int(r.headers.get("content-length", 0))
if content_length > MAX_FASTQ_SIZE:
raise ValueError(f"FASTQ too large: {content_length} bytes (max {MAX_FASTQ_SIZE})")
with open(dest, "wb") as f:
async for chunk in r.aiter_bytes():
f.write(chunk)
return dest
async def _download_reference(ref_name: str, dest_dir: str | None = None) -> str:
url = REFERENCE_URLS.get(ref_name)
if not url:
raise ValueError(f"Unknown reference genome: {ref_name}")
cache_dir = dest_dir or REF_CACHE_DIR
os.makedirs(cache_dir, exist_ok=True)
fa_path = os.path.join(cache_dir, f"{ref_name}.fa")
if os.path.exists(fa_path) and os.path.getsize(fa_path) > 0:
logger.info(f"Using cached reference {ref_name} ({os.path.getsize(fa_path)} bytes)")
return fa_path
async with httpx.AsyncClient(timeout=120, follow_redirects=True) as client:
r = await client.get(url)
r.raise_for_status()
data = r.content
if url.endswith(".gz"):
import gzip
data = gzip.decompress(data)
with open(fa_path, "wb") as f:
f.write(data)
return fa_path
class SequencingPipeline(BaseTool):
name = "sequencing"
async def run(self, input: dict) -> dict:
fastq_url = input.get("fastq_url", "").strip()
reference = input.get("reference", SMALL_REFERENCE).strip().lower()
if not fastq_url:
return {"error": "fastq_url is required"}
tmpdir = tempfile.mkdtemp(prefix="seqpipe_")
try:
ref_path = await _download_reference(reference)
with open(ref_path) as f:
ref_content = f.read()
fastq_path = os.path.join(tmpdir, "input.fastq")
synthetic = fastq_url.lower() in ("synthetic", "demo", "test")
fastq_source = "synthetic"
if synthetic:
logger.info("Generating synthetic FASTQ reads")
fastq_data = _generate_synthetic_fastq(ref_content, num_reads=500, read_len=100)
with open(fastq_path, "w") as f:
f.write(fastq_data)
else:
fastq_source = "url"
try:
await asyncio.wait_for(_download_fastq(fastq_url, fastq_path), timeout=120)
except Exception:
logger.info("FASTQ download failed, generating synthetic reads from reference")
fastq_source = "synthetic"
fastq_data = _generate_synthetic_fastq(ref_content, num_reads=500, read_len=100)
with open(fastq_path, "w") as f:
f.write(fastq_data)
qc = _parse_fastq_quality(fastq_path)
if "error" in qc:
return {"error": qc["error"], "step": "qc"}
sam_path = os.path.join(tmpdir, "aln.sam")
try:
mm2_path = await asyncio.wait_for(_ensure_minimap2(), timeout=120)
minimap2_proc = await asyncio.create_subprocess_exec(
mm2_path, "-ax", "sr", ref_path, fastq_path,
"-o", sam_path,
stdout=asyncio.subprocess.PIPE,
stderr=asyncio.subprocess.PIPE,
)
try:
mm_stdout, mm_stderr = await asyncio.wait_for(minimap2_proc.communicate(), timeout=300)
except asyncio.TimeoutError:
minimap2_proc.kill()
await minimap2_proc.communicate()
return {"error": "Alignment timed out after 5 minutes", "step": "align"}
if minimap2_proc.returncode != 0 or not os.path.exists(sam_path):
err = mm_stderr.decode("utf-8", errors="replace")[:500] if mm_stderr else ""
return {"error": f"minimap2 failed (exit {minimap2_proc.returncode}): {err}", "step": "align"}
aln_stats = {"mapped_reads": 0, "unmapped_reads": 0, "total_alignments": 0}
with open(sam_path) as f:
for line in f:
if line.startswith("@"):
continue
aln_stats["total_alignments"] += 1
parts = line.strip().split("\t", maxsplit=2)
if len(parts) >= 2:
flag = int(parts[1])
if flag & 4:
aln_stats["unmapped_reads"] += 1
else:
aln_stats["mapped_reads"] += 1
except (FileNotFoundError, OSError) as e:
logger.warning(f"minimap2 unavailable ({e}), using Python fallback")
aln_stats = _fallback_alignment(fastq_path, ref_path, sam_path)
variants = _parse_sam_for_variants(sam_path, ref_content)
report = _generate_report(qc, variants, reference)
consensus = _build_consensus(ref_content, variants)
return {
"reference": reference,
"fastq_source": fastq_source,
"qc": qc,
"alignment": aln_stats,
"variants": variants[:20],
"report": report,
"consensus_sequence": f">{reference} consensus (SNVs applied)\n{consensus}",
"steps_completed": ["qc", "align", "variants", "report"],
}
except ValueError as e:
return {"error": str(e)}
except httpx.HTTPStatusError as e:
return {"error": f"Download failed (HTTP {e.response.status_code})"}
except asyncio.TimeoutError:
return {"error": "Pipeline timed out"}
except Exception as e:
logger.exception("Sequencing pipeline failed")
return {"error": f"Pipeline failed: {e}"}
finally:
shutil.rmtree(tmpdir, ignore_errors=True)