python实现 提取gbk文件的登记码和ORIGIN序列

file_r = open("sequence.gbk")
file_w = open("sequence.fasta", "w")
flag = 0
for line in file_r:
    if line[0:9] == 'ACCESSION':
    #得到第一个空格和第二个空格之间的内容,[2]:得到第二个空格和第三个空格之间的内容
        AC = line.split()[1].strip() # AC = line.split( )[1]
        file_w.write('>'+AC + '\n')
    elif line[0:6] == 'ORIGIN':
        flag = 1
    elif flag == 1:
        fields = line.split()
        #[]不为空,!="",字符串不为空
        if fields != []:   
            seq = ''.join(fields[1:])#去掉列表中第一个元素(下标为0)的其他元素
            file_w.write(seq.upper() + '\n')#upper将小写字母转为大写字母
file_r.close()
file_w.close()

gbk文件:

LOCUS       DQ199648                 399 bp    mRNA    linear   PLN 01-OCT-2006
DEFINITION  Astragalus sinicus isolate AsE246 LTP-like protein 1 mRNA, complete
            cds.
ACCESSION   DQ199648
VERSION     DQ199648.1
KEYWORDS    .
SOURCE      Astragalus sinicus
  ORGANISM  Astragalus sinicus
            Eukaryota; Viridiplantae; Streptophyta; Embryophyta; Tracheophyta;
            Spermatophyta; Magnoliopsida; eudicotyledons; Gunneridae;
            Pentapetalae; rosids; fabids; Fabales; Fabaceae; Papilionoideae; 50
            kb inversion clade; NPAAA clade; Hologalegina; IRL clade; Galegeae;
            Astragalus.
REFERENCE   1  (bases 1 to 399)
  AUTHORS   Chou,M.-X., Wei,X.-Y. and Zhou,J.-C.
  TITLE     Identification of new nodulin cDNAs from Astragalus sinicus by SSH
  JOURNAL   Unpublished
REFERENCE   2  (bases 1 to 399)
  AUTHORS   Chou,M.-X., Wei,X.-Y. and Zhou,J.-C.
  TITLE     Direct Submission
  JOURNAL   Submitted (11-SEP-2005) National Key Laboratory of Agricultural
            Microbiology, Huazhong Agricultural University, Wuhan, Hubei
            430070, China
FEATURES             Location/Qualifiers
     source          1..399
                     /organism="Astragalus sinicus"
                     /mol_type="mRNA"
                     /isolate="AsE246"
                     /db_xref="taxon:47065"
     CDS             1..399
                     /codon_start=1
                     /product="LTP-like protein 1"
                     /protein_id="ABB13623.1"
                     /translation="MKFAYVVVVMCIMVVLNPSMTEAETISCREVVVTLTPCFPYLLS
                     GYGPSQSCCEAIKSFKIVFKNKINGQIACNCMKKAAFFGLSNANAEALPEKCNVKMHY
                     KINTSFDCTSIQDLKNVNVEKIQILQTLLV"
ORIGIN      
        1 atgaaatttg catatgtggt tgtggtgatg tgcatcatgg tagtgttgaa tccatccatg
       61 actgaggcag aaacaattag ttgccgtgaa gtggtggtga cgctcactcc ttgcttccca
      121 tatttgctta gtggttatgg tccatcccaa tcttgttgtg aagcaattaa gagtttcaaa
      181 attgtcttta aaaacaaaat taacggtcaa atcgcctgta attgtatgaa aaaagcagcg
      241 ttttttgggt tgagcaacgc taatgctgaa gcactccctg aaaaatgcaa tgtcaaaatg
      301 cactacaaga tcaacacatc cttcgactgt accagcatac aagatctaaa gaacgtgaat
      361 gtggagaaga ttcagatact tcaaactttg ttggtctag
//

结果文件:

>DQ199648
ATGAAATTTGCATATGTGGTTGTGGTGATGTGCATCATGGTAGTGTTGAATCCATCCATG
ACTGAGGCAGAAACAATTAGTTGCCGTGAAGTGGTGGTGACGCTCACTCCTTGCTTCCCA
TATTTGCTTAGTGGTTATGGTCCATCCCAATCTTGTTGTGAAGCAATTAAGAGTTTCAAA
ATTGTCTTTAAAAACAAAATTAACGGTCAAATCGCCTGTAATTGTATGAAAAAAGCAGCG
TTTTTTGGGTTGAGCAACGCTAATGCTGAAGCACTCCCTGAAAAATGCAATGTCAAAATG
CACTACAAGATCAACACATCCTTCGACTGTACCAGCATACAAGATCTAAAGAACGTGAAT
GTGGAGAAGATTCAGATACTTCAAACTTTGTTGGTCTAG
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可以使用Biopython和pandas库来解析基因组文件和gff3文件,并提取启动子序列。 首先,需要从基因组文件中读取DNA序列。假设基因组文件是fasta格式,可以使用Biopython中的SeqIO模块读取序列: ```python from Bio import SeqIO genome_file = "genome.fasta" genome_seq = SeqIO.read(genome_file, "fasta").seq ``` 接下来,需要从gff3文件提取基因信息和其位置。可以使用pandas库读取gff3文件,并筛选出基因信息: ```python import pandas as pd gff_file = "genome.gff3" gff_df = pd.read_csv(gff_file, sep="\t", comment="#", header=None) gff_df.columns = ["seqid", "source", "type", "start", "end", "score", "strand", "phase", "attributes"] gene_df = gff_df[gff_df["type"]=="gene"] ``` 然后,可以根据基因的位置提取其启动子序列。假设启动子长度为1000个碱基,可以根据基因的方向,从基因的上游或下游位置提取启动子序列: ```python upstream_len = 1000 promoter_seqs = [] for index, row in gene_df.iterrows(): gene_start = row["start"] gene_end = row["end"] gene_strand = row["strand"] if gene_strand == "+": promoter_start = max(gene_start - upstream_len, 0) promoter_end = gene_start else: promoter_start = gene_end promoter_end = gene_end + upstream_len if promoter_end > len(genome_seq): promoter_end = len(genome_seq) promoter_seq = genome_seq[promoter_start:promoter_end] promoter_seqs.append(promoter_seq) ``` 最后,可以将启动子序列保存到文件中: ```python with open("promoters.fasta", "w") as f: for i, promoter_seq in enumerate(promoter_seqs): f.write(">promoter_{}\n{}\n".format(i+1, promoter_seq)) ```

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