File: bigPsl.as

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table bigPsl
"bigPsl pairwise alignment"
(
   string          chrom;           "Reference sequence chromosome or scaffold"
   uint            chromStart;      "Start position in chromosome"
   uint            chromEnd;        "End position in chromosome"
   string          name;            "Name or ID of item, ideally both human readable and unique"
   uint            score;           "Score (0-1000)"
   char[1]         strand;          "+ or - indicates whether the query aligns to the + or - strand on the reference"
   uint            thickStart;      "Start of where display should be thick (start codon)"
   uint            thickEnd;        "End of where display should be thick (stop codon)"
   uint            reserved;        "RGB value (use R,G,B string in input file)"
   int             blockCount;      "Number of blocks"
   int[blockCount] blockSizes;      "Comma separated list of block sizes"
   int[blockCount] chromStarts;     "Start positions relative to chromStart"
   uint            oChromStart;     "Start position in other chromosome"
   uint            oChromEnd;       "End position in other chromosome"
   char[1]         oStrand;         "+ or -, - means that psl was reversed into BED-compatible coordinates"
   uint            oChromSize;      "Size of other chromosome."
   int[blockCount] oChromStarts;    "Start positions relative to oChromStart or from oChromStart+oChromSize depending on strand"
   lstring         oSequence;       "Sequence on other chrom (or edit list, or empty)"
   string          oCDS;            "CDS in NCBI format"
   uint            chromSize;       "Size of target chromosome"
   uint            match;           "Number of bases matched."
   uint            misMatch;        "Number of bases that don't match"
   uint            repMatch;        "Number of bases that match but are part of repeats"
   uint            nCount;          "Number of 'N' bases"
   uint            seqType;         "0=empty, 1=nucleotide, 2=amino_acid"
)