src/hg/encode/DAFs/WoldRnaSeq.daf 1.4

Index: src/hg/encode/DAFs/WoldRnaSeq.daf
===================================================================
RCS file: /projects/compbio/cvsroot/kent/src/hg/encode/DAFs/WoldRnaSeq.daf,v
retrieving revision 1.3
retrieving revision 1.4
diff -b -B -U 1000000 -r1.3 -r1.4
--- src/hg/encode/DAFs/WoldRnaSeq.daf	6 Mar 2009 00:52:10 -0000	1.3
+++ src/hg/encode/DAFs/WoldRnaSeq.daf	6 Mar 2009 16:53:30 -0000	1.4
@@ -1,97 +1,109 @@
 # Data Agreement File for RNA-seq project $Revision$
 
 # This file specifies the data agreement between your lab and 
 # the DCC.  It should not be changed unilaterally.
 
 # Lab and general info
 grant             Wold
 lab               Caltech
 dataType          RnaSeq
 variables         cell, localization, rnaExtract, mapAlgorithm, readType
 assembly          hg18
 dafVersion        0.2.2
 
 # Track/view definition
 view             Signal
 longLabelPrefix  Caltech RNA-Seq Map Algorithm Signal
 type             wig
 hasReplicates    no
 required         no
 
 view             RawSignal
 longLabelPrefix  Caltech RNA-Seq Raw Signal
 type             wig
 hasReplicates    yes
 required         no
 
 view             Splices
 longLabelPrefix  Caltech RNA-Seq Map Algorithm Splice Alignments
 type             bed 12
 hasReplicates    yes 
 required         no
 
 view             Aligns
 longLabelPrefix  Caltech RNA-Seq Map Algorithm Alignments
 type             bed 12
 hasReplicates    yes
 required         no
 
 view             Paired
 longLabelPrefix  Caltech RNA-Seq Map Algorithm Paired Alignments
 type             bed 12
 hasReplicates    yes
 required         no
 
 # For 2x75 datasets, raw Illumina reads (RawData, fasta format, query75.txt files) are run through bowtie 0.9.8.1 with up to 2 mismatches 
 # and the resulting mappings are stored (RawData2, bowtie format, hg18sp75spike.bowtie.txt files) for up to ten matches per-read to the genome, 
 # spiked controls and UCSC knownGene splice junctions. Reads that were not mapped by bowtie (RawData3, fasta format, unmapped.fa files) 
 # are then mapped onto the genome using blat and filtered using pslReps (RawData4, psl format, bowtierej.hg18.blatbetter files). 
 # The bowtie and blat mappings are then analyzed by ERANGE3.0.2 to generate wiggles (RawSignal, wiggle format, .graph files), 
 # bed files of all reads and splices (Aligns, PairedAligns, bed format, all.bed files), 
 # all bowtie and blat splices (Splices, bed format, allsplices.bed files), 
 # and blat-only splices (Splices, bed format, blatsplices.bed), 
 # as well as RPKM expression level measurements at the gene-level (RawData5, rpkm format, final.rpkm), 
 # exon-level (RawData6, rpkm format, gencode_exon.rpkm), and candidate novel exons (RawData7, rpkm format, accepted.rpkm).
 
 # query75.txt 
 view             RawData
 type             fasta
 hasReplicates    yes
 required         no
 
 # hg18sp75spike.bowtie.txt
 view             RawData2
 type             bowtie
 hasReplicates    yes
 required         no
 
 # unmapped.fa
 view             RawData3
 type             fasta
 hasReplicates    yes
 required         no
 
 # bowtierej.hg18.blatbetter
 view             RawData4
 type             psl
 hasReplicates    yes
 required         no
 
 # final.rpkm
 view             RawData5
 type             rpkm
 hasReplicates    yes
 required         no
 
 # gencode_exon
 view             RawData6
 type             rpkm
 hasReplicates    yes
 required         no
 
 # accepted.rpkm
 view             RawData7
 type             rpkm
 hasReplicates    yes
 required         no
 
+# hg18splice75.fa
+view             RawData8
+type             fasta
+hasReplicates    no
+required         no
+
+# spikes.fa
+view             RawData9
+type             fasta
+hasReplicates    no
+required         no
+