import pkg_resources import tempfile import magic import subprocess import tempfile import logging import re import io import gzip log = logging.getLogger(__name__ ) def read_fasta(sequence): entries = 0 bases = [] label = None for line in sequence: if line.startswith(">"): label = line entries += 1 else: bases.append(line) if entries > 1: log.debug("FASTA file contains multiple entries") raise ValueError("FASTA file contains multiple entries") return label, bases def qc_fasta(arg_sequence): log.debug("Starting qc_fasta") schema_resource = pkg_resources.resource_stream(__name__, "validation/formats") with tempfile.NamedTemporaryFile() as tmp: tmp.write(schema_resource.read()) tmp.flush() val = magic.Magic(magic_file=tmp.name, uncompress=False, mime=True) gz = "" if arg_sequence.name.endswith(".gz"): sequence = gzip.GzipFile(fileobj=arg_sequence, mode='rb') gz = ".gz" else: sequence = arg_sequence sequence = io.TextIOWrapper(sequence) r = sequence.read(4096) sequence.seek(0) seqlabel = r[1:r.index("\n")] seq_type = val.from_buffer(r).lower() if seq_type == "text/fasta": # ensure that contains only one entry submitlabel, submitseq = read_fasta(sequence) with tempfile.NamedTemporaryFile() as tmp1: refstring = pkg_resources.resource_string(__name__, "SARS-CoV-2-reference.fasta") tmp1.write(refstring) tmp1.write(submitlabel.encode("utf8")) tmp1.write(("".join(submitseq)).encode("utf8")) tmp1.flush() subbp = 0 refbp = 0 similarity = 0 try: cmd = ["clustalw", "-infile="+tmp1.name, "-quicktree", "-iteration=none", "-type=DNA"] print("QC checking similarity to reference") print(" ".join(cmd)) result = subprocess.run(cmd, stdout=subprocess.PIPE) res = result.stdout.decode("utf-8") g1 = re.search(r"^Sequence 1: [^ ]+ +(\d+) bp$", res, flags=re.MULTILINE) refbp = float(g1.group(1)) g2 = re.search(r"^Sequence 2: [^ ]+ +(\d+) bp$", res, flags=re.MULTILINE) subbp = float(g2.group(1)) g3 = re.search(r"^Sequences \(1:2\) Aligned\. Score: (\d+(\.\d+)?)$", res, flags=re.MULTILINE) similarity = float(g3.group(1)) print(g1.group(0)) print(g2.group(0)) print(g3.group(0)) except Exception as e: logging.warn("Error trying to QC against reference sequence using 'clustalw': %s", e) if refbp and (subbp/refbp) < .7: raise ValueError("QC fail: submit sequence length is shorter than 70% reference") if refbp and (subbp/refbp) > 1.3: raise ValueError("QC fail: submit sequence length is greater than 130% reference") if similarity and similarity < 70.0: raise ValueError("QC fail: submit similarity is less than 70%") if refbp == 0 or similarity == 0: raise ValueError("QC fail") return ("sequence.fasta"+gz, seqlabel) elif seq_type == "text/fastq": return ("reads.fastq"+gz, seqlabel) else: raise ValueError("Sequence file does not look like a DNA FASTA or FASTQ")