WormBase Tree Display for Sequence: F23A7

F23A7 DNA: F23A7 31520
  SMap: S_child (11)
  Structure: From: Source: CHROMOSOME_X
    Overlap_right: W10G6 31417
    Overlap_left: R11
    Clone_left_end: F23A7 1
      W10G6 31417
    Clone_right_end: R11 11652
  DB_info: Database: EMBL NDB_AC Z81067
        NDB_SV Z81067.2
    DB_remark: [121025] Sequence correction WBsf267946 : Insertion G1 bases from @ 9094
    Keyword: HTG
    EMBL_dump_info: EMBL_dump_method: worm_EMBL-dump
  Origin: From_author: McMurray AA
    From_laboratory: HX
    Date_directory: 960114
    Species: Caenorhabditis elegans
    Strain: WBStrain00000001
  Visible: Clone: F23A7
    Reference: WBPaper00015215
  Properties: Genomic_canonical
    Checksum: MD5: babdbcbf1d7295f0776c92974e5f600a
    Status: Finished: 14 Jan 1996 00:00:00
      Submitted: 21 Oct 1996 00:00:00
      Annotated: 15 Nov 1996 00:00:00
  Map: Sequence-X Ends: Left: 8817
        Right: 8831
  Interpolated_map_position: X 23.6969
  Assembly_tags: Finished Left 1 4 F23A7
    Clone left end 234 234 left hand end of F23A7
      1 4 left hand end of F23A7
      31417 31420 left hand end of W10G6
    annotation 12759 12778 This is a tentative join but we believe it is correct. The region from approx 12600bp to 13200bp has proved extremely difficult to sequence. PCR (from cosmid DNA) across this region gave the predicted band sizes.
      13036 13059 We have been unable to either double- strand or terminate this region (13,033 to 13,058 : approx 25bp). The available M13 clones are either deleted or slippage occurs during sequencing. Only ?Sequitherm? Taq with dye-primer sequencing gave good sequence on 2 M13 clones. Thermosequenase appeared to die completely when it hit this region. We think the sequence is correct and that there are no compressions across this 25bp
    Clone right end 11647 11652 right hand end of R11
    Finished Right 31517 31520 F23A7
  Method: Genomic_canonical