Schema for RefSeq Genes - BLAT Alignments of NCBI RefSeq Genes
  Database: DanaCAF1    Primary Table: refseqRNA    Row Count: 37,364   Data last updated: 2022-10-20
fieldexampleSQL type info
bin 585smallint(5) unsigned range
chrom scaffold_10000varchar(255) values
chromStart 3848int(10) unsigned range
chromEnd 4105int(10) unsigned range
name XR_004310392varchar(255) values
score 1000int(10) unsigned range
strand -char(1) values
thickStart 3848int(10) unsigned range
thickEnd 3848int(10) unsigned range
reserved 0int(10) unsigned range
blockCount 2int(10) unsigned range
blockSizes 125,59,longblob  
chromStarts 0,198,longblob  

Sample Rows
 
binchromchromStartchromEndnamescorestrandthickStartthickEndreservedblockCountblockSizeschromStarts
585scaffold_1000038484105XR_0043103921000-3848384802125,59,0,198,
585scaffold_1000945265020XR_004311427996-4526452602125,296,0,198,
585scaffold_1000945354821XR_004310395964-4535453502116,97,0,189,
585scaffold_1001116562224XR_0065079061000-165616560423,37,107,37,0,191,346,531,
585scaffold_1001117572224XR_0065079051000-175717570424,37,107,37,0,90,245,430,
585scaffold_1001117572231XR_0065079071000-175717570424,37,107,44,0,90,245,430,
585scaffold_1001710502010XR_004311337998-105010500464,143,110,195,0,449,653,765,
585scaffold_100391372613932XR_006508007962-137261372601206,0,
585scaffold_100501237XM_0324535391000+0118102810,369,0,868,
585scaffold_101033401383XM_014903521990-518122103319,346,325,0,372,718,

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

RefSeq Genes (refseqRNA) Track Description
 

Description

D. ananassae transcripts from the NCBI RefSeq database were aligned against the D. ananassae assembly using BLAT. The thicker boxes denote the coding regions within the transcripts and the thinner boxes denote the untranslated regions.

Methods

D. ananassae transcripts were mapped against the D. ananassae genome assembly using BLAT with the following parameters:

    -q=rna -fine -minScore=20 -stepSize=5

The transcript alignments are analyzed by pslReps using the following parameter:

    -minCover=0.15 -minAli=0.98 -nearTop=0.001

The alignments are then filtered by pslCDnaFilter using the following parameters:

    -minId=0.95 -minCover=0.15 -localNearBest=0.001 \
    -minQSize=20 -ignoreIntrons -repsAsMatch -ignoreNs -bestOverlap

References

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

The transcripts were obtained from the NCBI FTP site under the RefSeq assembly accession number GCF_017639315.1.