Manage projects and samples
In spacemake, each sample and its settings are stored in the project_df.csv under the root
directory of the spacemake project.
Each sample has exactly one row in this project_df.csv file. In the back-end, spacemake uses
a pandas.DataFrame to load and save this .csv file on disk. This data frame
is indexed by key (project-id, sample-id)
The spacemake class responsible for this back-end logic is the ProjectDF class.
Add a single sample
Sample parameters
In spacemake each sample can have the folloing variables:
project-idproject-idof a samplesample-idsample-idof a sampleR1.fastq.gzfile path(s) to Read1 read file(s). Can be either a single file, or a space separated list of consecutive files. If a list provided, the files will be merged together and the mergedR1.fastq.gzwill be processed downstream.R2same as before, but for Read2 read file(s).
longreads(optional)fastq(.gz)|fq(.gz)|bam file path to pacbio long reads for library debugging
longread-signature(optional)identify the expected longread signature (see longread.yaml)
dge(optional)Since the
0.1version of spacemake, it is possible to only provide the count matrix as input data for spacemake. Note: a raw count matrix is expected, if a non count matrix is provided, spacemake will raise an error.barcode-flavor(optional)barcode_flavorof the sample. If not provided,defaultwill be used (Drop-seq).speciesspeciesof the samplemap-strategyAs of version
0.7you can provide a mapping strategy as a string which gets converted into a series of map rules. These rules translate into BAM names and their dependencies.Example:
bowtie2:rRNA->STAR:genome:final
The input to the first mappings are always the pre-processed but unmapped reads. map-rules are composed of two or three paramters, separated by ‘:’. The first two parameters for the mapping are <mapper>:<reference>. The target BAM will have the name <reference>.<mapper>.bam. Supported mappers are currently bowtie2 and STAR The reference names must be defined for the species you assign to the sample.
Optionally, a triplet can be used <mapper>:<reference>:<symlink> where the presence of <symlink> indicates that the BAM file should additionally be made accessible under the name <symlink>.bam, a useful shorthand or common hook expected by other stages of SPACEMAKE. A special symlink name is “final” which is required by downstream stages of SPACEMAKE. If no “final” is specified, the last map-rule automatically is selected and symlinked as “final”. Note, due to the special importance of “final”, it may get modified to contain other flags of the run-mode that are presently essential for SPACEMAKE to have in the file name (“final.bam” may in fact be “final.polyA_adapter_trimmed.bam”)
The example above is going to create
rRNA.bowtie2.bam
using bowtie2 and the index associated with the “rRNA” reference
genome.STAR.bam
using STAR on the unmapped reads from BAM (1)
final.bam
a symlink pointing to the actual BAM created in (2).
Note that one BAM must be designated ‘final.bam’, or the last BAM file created will be selected as final. (used as input to downstream processing rules for DGE creation, etc.)
Note
Parallel mappings can be implemented by using commata:
bowtie2:rRNA:rRNA,STAR:genome:final
This rule differs from the first example because it will align the unmapped reads from the uBAM in parallel to the rRNA reference and to the genome. In this way the same reads can match to both indices.
Note
Gene tagging will be applied automatically if annotation data were provided for the associated reference index (by using ‘spacemake config add_species –annotation=… ‘)
Warning
Please be sure to escape your map_strategy with double-quotes to prevent bash from interpreting the ‘>’ as a redirect instruction.
puck(optional)name of the
puckfor this sample. if puck contains abarcodesvariable, with a path to a coordinate file, those coordinates will be used when processing this sample. If not provided, adefaultpuck will be used withwidth_um=3000,spot_diameter_um=10. For openst, you want to set this toopenst.puck-id(optional)puck-idof a samplepuck-barcode-file(optional)the path to the file contining (x,y) positions of the barcodes. If the
puckfor this sample has abarcodesvariable, it will be ignored, andpuck_barcode_filewill be used. For openst, you may initially add all the barcode files for the flowcell from which your capture area was made. Example:--puck-barcode-file /path/to/flowcell_barcode_files/fc*.txt.gzinvestigator(optional)name investigator(s) responsible for this sample
experiment(optional)description of the experiment
sequencing_date(optional)sequencing date of the sample
run_mode(optional)A list of
run_modenames for this sample. The sample will be processed as defined in therun_mode-s provided. If not provided, thedefaultrun_modewill be used.
To add a single sample, we can use the following command:
spacemake projects add-sample \
--project-id PROJECT-ID \ # required
--sample-id SAMPLE-ID \ # required
--R1 R1 [R1 R1 ...] \ # required, if no longreads
--R2 R2 [R2 R2 ...] \ # required, if no longreads
--longreads LONGREADS \ # required, if no R1 & R2
--longread-signature LONGREAD_SIGNATURE \ # optional
--barcode-flavor BARCODE_FLAVOR \ # optional
--species SPECIES \ # required
--puck PUCK \ # optional
--puck-id PUCK-ID \ # optional
--puck-barcode-file PUCK_BARCODE_FILE \ # optional
--investigator INVESTIGATOR \ # optional
--experiment EXPERIMENT \ # optional
--sequencing-date SEQUENCING_DATE \ # optional
--run-mode RUN_MODE [RUN_MODE ...] \ # optional
Warning
A sample is spatial only if: either a puck-barcode-file is provided, or the sample’s
puck has a barcodes variable pointing to a barcode position file.
If this is not the case, spacemake won’t be able to find the spatial barcodes for
this sample, and the sampe will be processed as a single-cell sample.
In case both the puck-barcode-file is provided and the sample’s puck has the
barcodes variable set, puck-barcode-file will be used for the spatial coordinates.
Note
As of version 0.9.3, spacemake can perform barcode correction if reference barcodes
are associated with a sample via --puck-barcode-file (see above). If no barcode files are
associated with your sample, no barcode correction will be performed and all reads will be mapped.
If barcode correction is possible, however, reads with non-matching barcodes will be dumped to
unaligned_bc_tagged.polyA_adapter_trimmed.nomatch.cram in the sample’s folder. Since these reads can not be spatially registered,
they can not be used in downstream analyses and do not need to be mapped.
Statistics and a graphical report on barcode matching can be found in the sample’s QC report.
Add a Visium/Seq-scope/Slide-seq sample
Currently spacemake works out of the box with three spatial methods: Visium, Seq-scope and Slide-seq.
To add a Visium sample, follow the quick start guide here.
To add a Seq-scope sample, follow the quick start guide here.
To add a Slide-seq sample, follow the quick start guide here.
Add a custom spatial sample
In order to process a custom spatial sample with spacemake follow the step by step guide below.
Step 1: specifying a puck
Each spatial sample will need a so-called puck to be configured first. By ‘puck’ we mean the physical properties of the underlying methods. Visium for instance works with 6.5mm by 6.5mm sized capture areas, where each spot has 55 microns diameter. To configure a custom puck follow the guide here.
Warning
If a puck is not specified, spacemake will still run but will use the default puck as specified here.
Step 2: formatting a custom puck-barcode-file
For all spatial samples we need to provide a puck_barcode_file. This file needs to be a comma or tab separated, and it needs to have the following three (named) columns:
cell_bc,barcodesorbarcodefor cell-barcode
xcoordorx_posfor x-positions
ycoordory_posfor y-positions
Step 3: configure run_mode(s), barcode_flavor and species
Before a custom sample is added the run_mode(s), barcode_flavor and species should be configured. The guides on how to do this can be found here for run-modes, here for and here for species.
The configured run_mode(s) will specify how a sample is processed downstream, and the barcode_flavor will specify the barcoding strategy used (ie how many nucleotides are used for UMI, which nucleotides are used for the spot barcodes).
Warning
If no run-mode(s) are provided spacemake will use the default run-mode as specified here.
Similarily if there is no barcode-flavor specified spacemake will use the default barcode-flavor as specified here.
Step 4: add your sample
Once everything is configured you can add your custom spatial sample with the following command:
spacemake projects add-sample \
# your sample's project-id \
--project-id PROJECT-ID \
# your sample's sample-id \
--sample-id SAMPLE-ID \
# one or more R1.fastq.gz files
--R1 R1 [R1 R1 ...] \
# one or more R2.fastq.gz files
--R2 R2 [R2 R2 ...] \
# name of the barcode-flavor, configured in Step 3 \
--barcode-flavor BARCODE_FLAVOR \
# name of the species, configured in Step 3 \
--species SPECIES \
# name of the puck, configured in Step 1 \
--puck PUCK \
# path to your custom barcode file, configured in Step 2 \
--puck-barcode-file PUCK_BARCODE_FILE \
# name of the run-mode(s), configured in Step 3 \
--run-mode RUN_MODE [RUN_MODE ...]
Add a single-cell sample
To add a single-cell sample follow the quick start guide here.
Add a pre-processed count-matrix
Coming soon!
Add several samples at once
It is possible to add several samples in just one command. First, the sample variables have
to be defined in a samples.yaml file, then we can run the following command:
spacemake projects add_samples_from_yaml --samples_yaml samples.yaml
The samples.yaml should have the following structure:
additional_projects:
- project-id: visium
sample-id: visium_1
R1: <path_to_visium_1_R1.fastq.gz>
R2: <path_to_visium_1_R2.fastq.gz>
species: mouse
puck: visium
barcode-flavor: visium
run-mode: [visium]
- project-id: visium
sample-id: visium_2
R1: <path_to_visium_2_R1.fastq.gz>
R2: <path_to_visium_2_R2.fastq.gz>
species: human
puck: visium
barcode-flavor: visium
run-mode: [visium]
- project-id: slideseq
sample-id: slideseq_1
R1: <path_to_slideseq_1_R1.fastq.gz>
R2: <path_to_slideseq_1_R2.fastq.gz>
species: mouse
puck: slideseq
barcode-flavor: slideseq_14bc
run-mode: [default, slideseq]
puck_barcode_file: <path_to_slideseq_puck_barcode_file>
Under additional_projects we define a list where each element will be a key:value pair, to be inserted in the project_df.csv
Note
When using the above command, if a sample is already present in the project_df.csv rather than adding it again, spacemake will update it.
If someone runs spacemake projects add-samples-from-yaml --samples yaml samples.yaml and
then modifies something in the samples.yaml, and runs the command again, the project_df.csv
will contain the updated version of the settings.
Add samples from an Illumina sample-sheet
You can add samples directly from an Illumina sample-sheet, assuming the sample-sheet is configured appropriately and a basecalls folder is available. Spacemake will then automatically process the sample-sheet, create the appropriate directories, and begin demultiplexing the data. Once the data is demultiplexed, spacemake will continue with the processing as described above.
To use this functionality, type:
spacemake projects add-sample-sheet \
--sample-sheet <path_to_sample_sheet> \
--basecalls-dir <path_to_basecalls_folder>
The sample-sheet columns have to obey certain conventions for spacemake to parse it properly:
Sample_IDcontains thesample-idin the project.Sample_Projectcontains theproject-idin the project.Descriptionmust end with_species, where species is the one configured for the samples in the project, e.g.HEK293_wt_human.
Spacemake will also parse the fields Investigator, Date, and Experiment from the sample-sheet and add them to the project metadata.
Listing projects
To list projects, which are already configured and added, simply type:
spacemake projects list
It will show the main variables for each project in the project_df.csv.
To view extra variables which are not shown, use the --variables option
to specify which extra variables to show.
Merging samples
Spacemake can merge samples that have been resequenced to increase the number of quantified
molecules in the data. To merge samples, first configure, add, and process the individual samples
as they are. Make sure that the samples belong in the same project, e.g. have the
same project-id. Then merge them by typing:
spacemake projects merge-samples \
--merge-project-id <project-id> \
--merged-sample-id <sample_merged> \
--sample-id-list <sample_a> <sample_b>
The above command will merge the two samples by creating a new sample with the same variables. Spacemake performs the merging at the level of the bam files, thus properly processing the merged sample by collapsing PCR duplicates. Processing will automatically run until the creation of the qc_sheets and the automated analyses.