Opened 9 years ago
Last modified 8 years ago
#887 closed task
Release export wizard — at Version 16
Reported by: | Nicklas Nordborg | Owned by: | Nicklas Nordborg |
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Priority: | critical | Milestone: | Reggie v4.5 |
Component: | net.sf.basedb.reggie | Keywords: | |
Cc: |
Description (last modified by )
Implement a wizard for creating all files that should be included in a release. Th wizard should take an item list with raw bioassays as input and produce a lot of files. Unless noted, all files are tab-separated text files.
- Transcript data (in folder
dataTables/transcriptDataTable
):tidmatrix.features.txt
: Array design features with some annotations. The first line is a header line:id
,geneSymbol
,refSeq
,protAcc
,description
,chr
,entrez
.- Rows are sorted by ID.
- All raw bioassays in the input list must use the same array design.
tidmatrix_data.txt
: FPKM values for all raw bioassays. Each row represents a feature and each column a raw bioassay.- The first line is a header line with raw bioassay names.
- The first column contains the feature ID.
- Same order of rows as the
tidmatrix.features.txt
.
tidmatrix_FPKM_conf_hi.txt
,tidmatrix_FPKM_conf_lo.txt
,tidmatrix_FPKM_status.txt
: More data files similar to thetidmatrix_data.txt
file but with theFPKM_conf_hi
,FPKM_conf_lo
andFPKM_status
values.
- Gene data (in folder
dataTables/geneDataTable
):genematrix_data.txt
: Sum of FPKM values per gene symbol.- The first line is a header line with raw bioassay names.
- The first column is the gene symbol (in
no particularalphabetical order).
is.NM.gene.txt
: TRUE/FALSE flag for each gene indicating if the refSeq ID starts withNM_
or not.- No header line.
- First column is the line number (in this file, add +1 for getting the line number in
genematrix_data.txt
). - Second column is
TRUE
orFALSE
.
- Cohort data (in folder
cohortTables
): A set of tab-separated files with data for each raw bioassay and the parent items it is derived from. Each file starts with a header line. Each row contains data for one raw bioassay. The first column (rba
) is always the name of the raw bioassay. Columns ending with.A.
are annotation columns. Date values are formatted asYYYY-MM-DD
unless otherwise noted.cohortRawbioassay.txt
: Data from the raw bioassay level. Columns:ID
: Internal ID in BASEName
: Name of raw bioassayPlatform
: Name of platform (Sequencing)Raw.data.type
: Name of raw data type (cufflinks)Has.data
: Flag indicating if there is raw data for this raw bioassay or not (TRUE/FALSE)Db.spots
: Number of raw data entriesArray.design
: Name of the array designSoftware
: Name of the software used to generate the raw dataImport.date
: Date the raw data was createdAnalysisResult..A.
DataFilesFolder..A.
FPKM.tracking.file..F.
: Path to theisoforms.fpkm_tracking
file in the BASE file system
cohortAligned.txt
: Data from theAlignedSequences
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (AlignedSequences)Software
: Name of the software used for alignmentRegistered
: Date the item was registered in BASEAnalysisResult..A.
DataFilesFolder..A.
ALIGNED_PAIRS..A.
READ_PAIRS_EXAMINED..A.
READ_PAIR_DUPLICATES..A.
cohortMasked.txt
: Data from theMaskedSequences
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (MaskedSequences)Software
: Name of the software used for maskingRegistered
: Date the item was registered in BASEPM_READS..A.
cohortMerged.txt
: Data from theMergedSequences
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (MergedSequences)Physical.bioassays
: Name of the physical bioassay (flow cell) used for sequencing. Comma-separated list if there is more than one.Software
: Name of the software used for mergingRegistered
: Date the item was registered in BASEAnalysisResult..A.
DataFilesFolder..A.
READS..A.
PF_READS..A.
ADAPTER_READS..A.
PT_READS..A.
FragmentSizeAvg..A.
FragmentSizeStdev..A.
cohortSequencing.txt
: Data from theSequencingRun
parent item. Columns:- TODO
cohortLibrary.txt
: Data from theLibrary
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (Library)Protocol
: Name of the library preparation protocolCreated
: Date the library was createdTag
: Name of the barcode used by the libraryBioplate
: Name of the library plateBiowell.row
: Row coordinate on the library plate (A-H)Biowell.column
: Column coordinate on the library plate (1-12)QubitConc..A.
cohortRNA.txt
: Data from theRNA
/RNAQC
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (RNA)Original.quantity..µg.
: µg RNA that was extractedNDConc..A.
ND260by230..A.
ND260by280..A.
QiacubeDate..A.
QiacubeRunNo..A.
QiacubePosition..A.
RNAQC_last
: RIN/RQS value from the latest quality control
cohortLysate.txt
: Data from theLysate
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (Lysate)Created
: Date the lysate was createdOriginal.quantity..µg.
: µg Lysate that was extractedParent.items
: Name and used quantity from the specimenMultPieces..A.
PartitionDate..A.
cohortSample.txt
: Data from theSpecimen
parent item. Columns:ID
: Internal ID in BASEName
: Name of itemType
: Type of item (Lysate)Original.quantity..µg.
: Weight of sample receivedCreated
: Date the sample was created (operation date)ArrivalDate..A.
BiopsyType..A.
SpecimenType..A.
Laterality..A.
NofDeliveredTubes..A.
NofPieces..A.
OperatorDeliveryComment..A.
OperatorPartitionComment..A.
SamplingDateTime..A.
RNALaterDateTime..A.
LinkedSpecimen..A.
cohortCase.txt
: Data from theCase
parent item (except INCA data). Columns:- TODO
cohortPatient.txt
: Data from thePatient
parent item. Columns:- TODO
cohortStained.txt
: Data from theStained
parent item. Columns:- TODO
cohortINCA.txt
: Data from parent items (eg. Case) that have been imported from the INCA registry. Columns:- TODO
cohortSummaryTable.txt
: A single table collecting some of the most useful information from the other tables.
- Subtype data (in folder
cohortTables/subtypeTables
): Information generated by the R report scripts. We do not currently store this information in BASE, so it needs to be discussed how this should be done. The report plug-in could for example import the data from the R scripts as annotations.
- README files
- TODO
Change History (16)
comment:1 by , 9 years ago
Description: | modified (diff) |
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comment:2 by , 9 years ago
Description: | modified (diff) |
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comment:3 by , 9 years ago
Description: | modified (diff) |
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comment:4 by , 9 years ago
Status: | new → assigned |
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comment:5 by , 9 years ago
Description: | modified (diff) |
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comment:6 by , 9 years ago
Description: | modified (diff) |
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comment:7 by , 9 years ago
Description: | modified (diff) |
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comment:8 by , 9 years ago
Description: | modified (diff) |
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comment:9 by , 9 years ago
Milestone: | Reggie v4.x → Reggie v4.5 |
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comment:10 by , 9 years ago
(In [3932]) References #887: Release export wizard
Created the exporter plug-in (ReleaseExporterPlugin
). This is a front-end for interacting with the user. The plug-in is installed in the "Item list" toolbar and asks for an output directory and if existing files should be overwritten or not.
The actual export is going to be implemented in the ReleaseExporter
class. It is currently only able to collect the parameters and make some checks on the rawbioassays/array design.
comment:11 by , 9 years ago
comment:12 by , 9 years ago
(In [3934]) References #887: Release export wizard
Implemented exporter for th transcript data. Eg. all remaining files in the dataTables/transcriptDataTable
directory.
Note that the current implementation only export data from the first raw bioassay. BASE 3.9 is needed to be able to export from all raw bioassays.
comment:13 by , 9 years ago
(In [3935]) References #887: Release export wizard
Started with the cohort exporters. The CohortItem
is used for loading all information related to a single raw bioassays. It is used and then discarded in smaller batches to let garbage collection clean up memory.
The CohortWriter
is an extension to the ReleaseWriter
for writing cohort data. Each cohort data file need a subclass. The RawBioAssayWriter
is the first such writer that write the raw bioassay data.
comment:14 by , 9 years ago
comment:15 by , 9 years ago
comment:16 by , 9 years ago
Description: | modified (diff) |
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For efficient calculations it is desirable to process the data gene symbol by gene symbol. Thus, the data must come sorted in gene symbol order.