Automatic Data Aggregation
When launching apps that use biosamples as inputs, BaseSpace Sequence Hub automatically aggregates all of the valid (QC Passed) FASTQ data for the biosample. You can control which data are used in analyses by setting the QC status of a resource as QC Passed or QC Failed.
If a biosample was converted from a sample and has data produced by two or more runs, it is automatically locked. The data cannot be used in analysis until the biosample has been reviewed and unlocked, however you can switch to Classic mode to launch analyses using the original sample data without aggregation. For information about unlocking biosamples to make them available for analysis, see Unlock Biosamples.
You do not need to merge biosamples to combine their data for analysis.
When BaseSpace Sequence Hub collects data for an app launch, it automatically excludes QC Failed lanes, libraries, pools, and any downstream data they produced. For example, if you fail a flow cell lane, all FASTQ data sets produced from that lane are excluded when aggregating data for the biosamples and libraries put on those lanes. If you fail a FASTQ dataset, only that FASTQ dataset is excluded.
If a FASTQ dataset has been copied, BaseSpace Sequence Hub uses the original FASTQ dataset, or the most recent copy if the original is not available. If you wish to use a different copy, mark the other copies as QC Failed before starting the analysis.
The following resources can be excluded from data aggregation:
|•||Lanes—Fail lanes using Automatic Lane QC, BaseSpace Sequence Hub API, or manually in BaseSpace Sequence Hub.|
|•||Libraries—Fail libraries using the BaseSpace Sequence Hub API.|
|•||Pools—Fail pools using the BaseSpace Sequence Hub API.|
|•||FASTQ Datasets—Fail FASTQ data sets using the BaseSpace Sequence Hub API, or manually in BaseSpace Sequence Hub.|
BaseSpace Sequence Hub aggregates FASTQ data sets with different read lengths from the same biosample.
When using apps that have not been updated to use biosamples or data sets as inputs, BaseSpace Sequence Hub automatically converts the FASTQ data sets into samples before launching the app.
When you schedule an analysis, you can specify the Prep Kit with the input biosample. The analysis launches using only FASTQ datasets from libraries of the specified Prep Kit. In the following example, Prep Kit B is selected as input and the FASTQ files from Prep Kit A are excluded.