Schema for fRNAdb::EvoFold - fRNAdb::EvoFold track
Database: hg19    Primary Table: F_EvoFold    Row Count: 47,802
fieldexampleSQL type info
bin 1284smallint(5) unsigned range
matches 42int(10) unsigned range
misMatches 0int(10) unsigned range
repMatches 0int(10) unsigned range
nCount 0int(10) unsigned range
qNumInsert 0int(10) unsigned range
qBaseInsert 0int(10) unsigned range
tNumInsert 0int(10) unsigned range
tBaseInsert 0int(10) unsigned range
strand +char(2) values
qName FR197792varchar(255) values
qSize 42int(10) unsigned range
qStart 0int(10) unsigned range
qEnd 42int(10) unsigned range
tName chr7varchar(255) values
tSize 159138663int(10) unsigned range
tStart 91739922int(10) unsigned range
tEnd 91739964int(10) unsigned range
blockCount 1int(10) unsigned range
blockSizes 42,longblob  
qStarts 0,longblob  
tStarts 91739922,longblob  
Sample Rows
binmatchesmisMatchesrepMatchesnCountqNumInsertqBaseInserttNumInserttBaseInsertstrandqNameqSizeqStartqEndtNametSizetStarttEndblockCountblockSizesqStartstStarts
1284420000000+FR19779242042chr71591386639173992291739964142,0,91739922,
1961450000000-FR39916345045chr3198022430180462296180462341145,0,180462296,
944240000000-FR19040724024chrX1552705604707241647072440124,0,47072416,
1116250000000+FR29711625025chr16903547536967917369679198125,0,69679173,
1535240000000+FR18055024024chr6171115067124639171124639195124,0,124639171,
794150000000-FR01887315015chr17811952102742335327423368115,0,27423353,
1358180000000+FR06151318018chr7159138663101421482101421500118,0,101421482,
788340000000+FR34144434034chr71591386632672934126729375134,0,26729341,
966290000000+FR23856029029chr101355347474994711849947147129,0,49947118,
1321190000000+FR30134019019chr12492506219647575396475772119,0,96475753,

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

fRNAdb::EvoFold (F_EvoFold) Track Description

Description

This track shows conserved non-coding regions predicted by EvoFold [1].

This track is prepared to give interoperability with the functional RNA database [2] v3.0.

Methods

Short sequences (shorter than 30nt) are aligned to genome by SeqMap [3] with 0 mismatch, no-gap and no-repeat.

Other sequences are aligned to genome by BLAT [4] with identity>=99, coverage>=90 and no-repeat.

And limit results to positions of EvoFold track in UCSC Genome Browser.

References

  [1] Pedersen JS, Bejerano G, Siepel A, Rosenbloom K, Lindblad-Toh K, Lander ES, Kent J, Miller W, Haussler D.
      Identification and classification of conserved RNA secondary structures in the human genome.
      PLoS Comput Biol. 2006 Apr;2(4):e33.
  [2] Kin T, Yamada K, Terai G, Okida H, Yoshinari Y, Ono Y, Kojima A, Kimura Y, Komori T, Asai K.
      fRNAdb: a platform for mining/annotating functional RNA candidates from non-coding RNA sequences.
      Nucleic Acids Res. 2007 Jan;35(Database issue):D145-8.
  [3] Jiang H, Wong WH
      SeqMap: mapping massive amount of oligonucleotides to the genome.
      Bioinformatics. 2008 Oct 15;24(20):2395-6. Epub 2008 Aug 12.
  [4] Kent WJ.
      BLAT--the BLAST-like alignment tool.
      Genome Res. 2002 Apr;12(4):656-64.