Schema for xenoMrna
  Database: macEug2    Primary Table: xenoMrna    Row Count: 6,759,450   Data last updated: 2016-02-16
On download server: MariaDB table dump directory
fieldexampleSQL type
bin 585smallint(5) unsigned
matches 140int(10) unsigned
misMatches 41int(10) unsigned
repMatches 0int(10) unsigned
nCount 0int(10) unsigned
qNumInsert 0int(10) unsigned
qBaseInsert 0int(10) unsigned
tNumInsert 0int(10) unsigned
tBaseInsert 0int(10) unsigned
strand ++char(2)
qName JI430307varchar(255)
qSize 393int(10) unsigned
qStart 210int(10) unsigned
qEnd 391int(10) unsigned
tName ABQO010000375varchar(255)
tSize 938int(10) unsigned
tStart 551int(10) unsigned
tEnd 732int(10) unsigned
blockCount 1int(10) unsigned
blockSizes 181,longblob
qStarts 210,longblob
tStarts 551,longblob

Connected Tables and Joining Fields
        hgFixed.gbCdnaInfo.acc (via xenoMrna.qName)
      hgFixed.gbMiscDiff.acc (via xenoMrna.qName)
      hgFixed.gbSeq.acc (via xenoMrna.qName)
      hgFixed.gbWarn.acc (via xenoMrna.qName)
      hgFixed.imageClone.acc (via xenoMrna.qName)
      macEug2.all_est.qName (via xenoMrna.qName)
      macEug2.all_mrna.qName (via xenoMrna.qName)
      macEug2.xenoRefFlat.name (via xenoMrna.qName)
      macEug2.xenoRefGene.name (via xenoMrna.qName)
      macEug2.xenoRefSeqAli.qName (via xenoMrna.qName)

Sample Rows
 
binmatchesmisMatchesrepMatchesnCountqNumInsertqBaseInserttNumInserttBaseInsertstrandqNameqSizeqStartqEndtNametSizetStarttEndblockCountblockSizesqStartstStarts
58514041000000++JI430307393210391ABQO0100003759385517321181,210,551,
58514058000000+-JP3281081063509707ABQO0100003759385517491198,509,189,
58510644000000++HP503938523337487ABQO0100003759385527021150,337,552,
58511247000000++HP479561453293452ABQO0100003759385527111159,293,552,
58511451000000++JP344452618433598ABQO0100003759385527171165,433,552,
58516020000000++JI895261929748928ABQO0100003759385527321180,748,552,
58516020000000++JP043533929748928ABQO0100003759385527321180,748,552,
58515048000000++AK17472273214212ABQO0100003759385527501198,14,552,
58514354000011++CU67913511108421039ABQO0100003759385527502128,69,842,970,552,681,
5857335000000+-JO680000629519627ABQO0100003759386087161108,519,222,

Note: all start coordinates in our database are 0-based, not 1-based. See explanation here.

Other mRNAs (xenoMrna) Track Description
 

Description

This track displays translated blat alignments of vertebrate and invertebrate mRNA in GenBank from organisms other than human.

Display Conventions and Configuration

This track follows the display conventions for PSL alignment tracks. In dense display mode, the items that are more darkly shaded indicate matches of better quality.

The strand information (+/-) for this track is in two parts. The first + indicates the orientation of the query sequence whose translated protein produced the match (here always 5' to 3', hence +). The second + or - indicates the orientation of the matching translated genomic sequence. Because the two orientations of a DNA sequence give different predicted protein sequences, there are four combinations. ++ is not the same as --, nor is +- the same as -+.

The description page for this track has a filter that can be used to change the display mode, alter the color, and include/exclude a subset of items within the track. This may be helpful when many items are shown in the track display, especially when only some are relevant to the current task.

To use the filter:

  1. Type a term in one or more of the text boxes to filter the mRNA display. For example, to apply the filter to all mRNAs expressed in a specific organ, type the name of the organ in the tissue box. To view the list of valid terms for each text box, consult the table in the Table Browser that corresponds to the factor on which you wish to filter. For example, the "tissue" table contains all the types of tissues that can be entered into the tissue text box. Multiple terms may be entered at once, separated by a space. Wildcards may also be used in the filter.
  2. If filtering on more than one value, choose the desired combination logic. If "and" is selected, only mRNAs that match all filter criteria will be highlighted. If "or" is selected, mRNAs that match any one of the filter criteria will be highlighted.
  3. Choose the color or display characteristic that should be used to highlight or include/exclude the filtered items. If "exclude" is chosen, the browser will not display mRNAs that match the filter criteria. If "include" is selected, the browser will display only those mRNAs that match the filter criteria.

This track may also be configured to display codon coloring, a feature that allows the user to quickly compare mRNAs against the genomic sequence. For more information about this option, go to the Codon and Base Coloring for Alignment Tracks page. Several types of alignment gap may also be colored; for more information, go to the Alignment Insertion/Deletion Display Options page.

Methods

The mRNAs were aligned against the human genome using translated blat. When a single mRNA aligned in multiple places, the alignment having the highest base identity was found. Only those alignments having a base identity level within 1% of the best and at least 25% base identity with the genomic sequence were kept.

Credits

The mRNA track was produced at UCSC from mRNA sequence data submitted to the international public sequence databases by scientists worldwide.

References

Benson DA, Cavanaugh M, Clark K, Karsch-Mizrachi I, Lipman DJ, Ostell J, Sayers EW. GenBank. Nucleic Acids Res. 2013 Jan;41(Database issue):D36-42. PMID: 23193287; PMC: PMC3531190

Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Wheeler DL. GenBank: update. Nucleic Acids Res. 2004 Jan 1;32(Database issue):D23-6. PMID: 14681350; PMC: PMC308779

Kent WJ. BLAT - the BLAST-like alignment tool. Genome Res. 2002 Apr;12(4):656-64. PMID: 11932250; PMC: PMC187518