Fc int2

tests/integration_1/pipeline.yml

@@ -0,0 +1,390 @@
+# Pipeline pipeline_integration.py configuration file
+# ==============================================
+
+# compute resource options
+# ------------------------
+resources:
+  # Number of threads used for parallel jobs
+  # this must be enough memory to load your mudata and do computationally intensive tasks
+  threads_high: 1
+  # this must be enough memory to load your mudata and do computationally light tasks
+  threads_medium: 1
+  # this must be enough memory to load text files and do plotting, requires much less memory than the other two
+  threads_low: 1
+  # if you access to a gpu-specific queue, how many gpu threads to request, make sure to edit the queues section below,
+  # so that panpipes can find your gpu queue
+  threads_gpu: 2
+# path to conda env, leave blank if running native or your cluster automatically inherits the login node environment
+condaenv: /Users/fabiola.curion/Documents/devel/miniconda3/envs/pipeline_env
+
+# allows for tweaking which queues jobs get submitted to, 
+# in case there is a special queue for long jobs or you have access to a gpu-specific queue
+# the default queue should be specified in your .cgat.yml file
+# leave blank if you do not want to use the alternative queues
+queues:
+  long: 
+  gpu:  
+
+# Start
+# --------------------------
+# either one that exists already with
+sample_prefix: teaseq
+#this is what comes out of the filtering/preprocessing
+preprocessed_obj: teaseq.h5mu
+# contains layers: raw_counts, logged_counts, and has scaled or logged counts in X 
+
+
+#--------------------------
+# Batch correction
+# -------------------------
+# unimodal: correct each modality independently
+rna:
+  # True or false depending on whether you want to run batch correction
+  run: False 
+  # what method(s) to use to run batch correction, you can specify multiple 
+  # choices: harmony,bbknn,scanorama,scvi (comma-seprated string, no spaces)
+  tools: harmony,scvi,bbknn
+  # this is the column you want to batch correct on. if you specify a comma separated list, 
+  # they will be all used simultaneosly. 
+  # Specifically all columns specified will be merged into one 'batch' columns.
+  # if you want to test correction for one at a time, 
+  # specify one at a time and run the pipeline in different folders i.e. integration_by_sample, 
+  # integration_by_tissue ...
+  column: dataset
+  #-----------------------------
+  # Harmony args
+  #-----------------------------
+  harmony:
+  # sigma value, used by Harmony
+    sigma: 0.1 
+  # theta value used by Harmony, default is 1
+    theta: 1.0
+  # number of pcs, used by Harmony
+    npcs: 30
+  #----------------------------
+  # BBKNN args # https://bbknn.readthedocs.io/en/latest/
+  #-----------------------------
+  bbknn:
+    neighbors_within_batch: 20
+  #-----------------------------
+  # SCVI args
+  #-----------------------------
+  scvi:
+    exclude_mt_genes: True
+    mt_column: mt
+    model_args:
+        n_layers: 
+        n_latent:
+        gene_likelihood: zinb
+    training_args:
+        max_epochs: 400
+        train_size: 0.9
+        early_stopping: True
+    training_plan: 
+        lr: 0.001
+        n_epochs_kl_warmup: 400
+        reduce_lr_on_plateau: True
+        lr_scheduler_metric: 
+        lr_patience: 8
+        lr_factor: 0.1
+  #----------------------------
+  # find neighbour parameters
+  #-----------------------------
+  # to reuse these params, (for example for WNN) please use anchors (&) and scalars (*) in the relevant place
+  # i.e. &rna_neighbors will be called by *rna_neighbors where referenced
+  neighbors: &rna_neighbors 
+  # number of Principal Components to calculate for neighbours and umap:
+  #   -if no correction is applied, PCA will be calculated and used to run UMAP and clustering on
+  #   -if Harmony is the method of choice, it will use these components to create a corrected dim red.)
+  # the maximum number of dims for neighbors calculation can only only be lower or equal to the total number of dims for PCA or Harmony
+  # note: scvelo default is 30
+    npcs: 30
+    # number of neighbours
+    k: 30
+    # metric: euclidean | cosine
+    metric: euclidean
+    # scanpy | hnsw (from scvelo)
+    method: scanpy
+
+#--------------------------
+prot:
+  # True or false depending on whether you want to run batch correction
+  run: False 
+  # what method(s) to use to run batch correction, you can specify multiple 
+  # choices: harmony,bbknn,combat
+  tools: harmony
+  # this is the column you want to batch correct on. if you specify a comma separated list (no spaces), 
+  # they will be all used simultaneosly. if you want to test correction for one at a time, 
+  # specify one at a time and run the pipeline in different folders i.e. integration_by_sample, 
+  # integration_by_tissue ...
+  column: orig.ident 
+  #----------------------------
+  # Harmony args
+  #-----------------------------
+  harmony:
+  # sigma value, used by Harmony
+    sigma: 0.1 
+  # theta value used by Harmony, default is 1
+    theta: 1.0
+  # number of pcs, used by Harmony
+    npcs: 30
+  #----------------------------
+  # BBKNN args # https://bbknn.readthedocs.io/en/latest/
+  #-----------------------------
+  bbknn:
+    neighbors_within_batch: 20
+  #----------------------------›
+  # find neighbour parameters
+  #-----------------------------
+  neighbors: &prot_neighbors
+    # number of Principal Components to calculate for neighbours and umap:
+    #   -if no correction is applied, PCA will be calculated and used to run UMAP and clustering on
+    #   -if Harmony is the method of choice, it will use these components to create a corrected dim red.)
+    # note: scvelo default is 30
+    npcs: 30
+    # number of neighbours
+    k: 30
+    # metric: euclidean | cosine
+    metric: euclidean
+    # scanpy | hnsw (from scvelo)
+    method: scanpy
+#--------------------------
+atac:
+  # True or false depending on whether you want to run batch correction
+  run: True
+  # which dimensionality reduction to expect, LSI or PCA
+  dimred: LSI 
+  # what method(s) to use to run batch correction, you can specify multiple 
+  # (comma-seprated string, no spaces)
+  # choices: harmony,bbknn,combat
+  tools: harmony,bbknn
+  # this is the column you want to batch correct on. if you specify a comma separated list, 
+  # they will be all used simultaneosly. if you want to test correction for one at a time, 
+  # specify one at a time and run the pipeline in different folders i.e. integration_by_sample, 
+  # integration_by_tissue ...
+  column: dataset
+  #----------------------------
+  # Harmony args
+  #-----------------------------
+  harmony:
+  # sigma value, used by Harmony
+    sigma: 0.1 
+  # theta value used by Harmony, default is 1
+    theta: 1.0
+  # number of pcs, used by Harmony
+    npcs: 30
+  #----------------------------
+  # BBKNN args # https://bbknn.readthedocs.io/en/latest/
+  #-----------------------------
+  bbknn:
+    neighbors_within_batch: 30
+  #----------------------------
+  # find neighbour parameters
+  #-----------------------------
+  neighbors: &atac_neighbors
+    # number of Principal Components to calculate for neighbours and umap:
+    #   -if no correction is applied, PCA will be calculated and used to run UMAP and clustering 
+    #   -if Harmony is the method of choice, it will use these components to create a corrected dim red.)
+    # note: scvelo default is 30
+    npcs: 30
+    # number of neighbours
+    k: 30
+    # metric: euclidean | cosine
+    metric: euclidean
+    # scanpy | hnsw (from scvelo)
+    method: scanpy
+#----------------------------------------------
+# multimodal integration
+# remember to specify knn graph params in the section "neighbors"
+#----------------------------------------------
+multimodal:
+  # True or false depending on whether you want to run batch correction
+  run: True 
+  # what method(s) to use to run batch correction, you can specify multiple 
+  # choices: totalvi, mofa, MultiVI, WNN
+  # list e.g. below
+  tools: 
+    - MultiVI
+
+  # this is the column you want to batch correct on. if you specify a comma separated list, 
+  # they will be all used simultaneosly. if you want to test correction for one at a time, 
+  # specify one at a time and run the pipeline in different folders i.e. integration_by_sample, 
+  # integration_by_tissue ...
+  column_continuous: 
+  column_categorical: dataset
+  # extra params:
+  totalvi:
+    # this is a minimal set of parameters that will be expected
+    # you can add any other param from the tutorials and they will
+    # be parsed alongside the others
+
+    # totalvi will run on rna and prot
+    modalities: rna,prot
+    exclude_mt_genes: True
+    mt_column: mt
+    # to filter outliers manually create a column called adt_outliers in mdata['prot'].obs
+    filter_by_hvg: True
+    filter_prot_outliers: False
+    model_args: 
+      latent_distribution: "normal"
+    training_args:
+      max_epochs: 100
+      train_size: 0.9
+      early_stopping: True
+    training_plan: None
+  MultiVI:
+    # this is a minimal set of parameters that will be expected
+    # you can add any other param from the tutorials and they will
+    # be parsed alongside the others
+    # leave arguments blank for default
+    lowmem: True
+    # Set lowmem to True will subset the atac to the top 25k HVF. 
+    # This is to deal with concatenation of atac,rna on large datasets which at the moment is suboptimally required by scvitools.
+    # >100GB of RAM are required to concatenate atac,rna with 15k cells and 120k total features (union rna,atac)
+    model_args:
+      # (default: None)
+      n_hidden :  
+      # (default: None)
+      n_latent :  
+      #(bool,default: True)
+      region_factors : True 
+       #{‘normal’, ‘ln’} (default: 'normal')
+      latent_distribution : 'normal'
+      #(bool,default: False)
+      deeply_inject_covariates : False 
+      #(bool, default: False)
+      fully_paired : False 
+    training_args:
+      #(default: 500)
+      max_epochs : 500 
+      #float (default: 0.0001)
+      lr : 1.0e-05
+      #leave blanck for default str | int | bool | None (default: None)
+      use_gpu :
+      # float (default: 0.9)
+      train_size : 0.9 
+      # leave blanck for default, float | None (default: None)
+      validation_size : 
+      # int (default: 128)
+      batch_size : 128
+      #float (default: 0.001)
+      weight_decay : 0.001 
+      #float (default: 1.0e-08)
+      eps : 1.0e-08 
+      #bool (default: True)
+      early_stopping : True 
+      #bool (default: True)
+      save_best : True
+       #leave blanck for default int | None (default: None)
+      check_val_every_n_epoch :
+      #leave blanck for default int | None (default: None)
+      n_steps_kl_warmup : 
+       # int | None (default: 50)
+      n_epochs_kl_warmup : 50
+      #bool (default: True)
+      adversarial_mixing : True 
+       #leave blanck for default dict | None (default: None)
+    training_plan :
+  mofa:
+    # this is a minimal set of parameters that will be expected
+    # you can add any other param from the tutorials and they will
+    # be parsed alongside the others
+    #  (comma-separated string, no spaces)
+    modalities: 
+    filter_by_hvg: True
+    n_factors: 10
+    n_iterations: 1000
+    #pick one among fast, medium, slow
+    convergence_mode: fast
+    save_parameters: False
+    #if save_parameters True, set the following, otherwise leave blank
+    outfile: 
+  WNN:
+    # muon implementation of WNN 
+    modalities: rna,prot,atac 
+    # run wnn on batch corrected unimodal data, set each of the modalities you want to use to calc WNN to ONE method.
+    # leave to None and it will default to de novo calculation of neighbours on non corrected data for that modality using specified params 
+    batch_corrected:
+      # options are: "bbknn", "scVI", "harmony", "scanorama"
+      rna: None
+      # options are "harmony", "bbknn"
+      prot: None
+      # options are "harmony"
+      atac: None 
+    # please use anchors (&) and scalars (*) in the relevant place
+    # i.e. &rna_neighbors will be called by *rna_neighbors where referenced
+    knn:
+      rna: *rna_neighbors
+      prot: *prot_neighbors
+      atac: *atac_neighbors
+    #WNN has its own neighbors search, specify here  
+    n_neighbors: #leave blank and it will default to aritmetic mean across modalities neighbors
+    n_bandwidth_neighbors: 20
+    n_multineighbors: 200
+    metric: 'euclidean'
+    low_memory: True
+
+  ###
+  # neighbours knn calculation for multimodal analysis. 
+  ###
+  neighbors:
+    # number of Principal Components to calculate for neighbours and umap:
+    #   -if no correction is applied, PCA will be calculated and used to run UMAP and clustering on
+    #   -if Harmony is the method of choice, it will use these components to create a corrected dim red.)
+    # note: scvelo default is 30
+    npcs: 30
+    # number of neighbours
+    k: 30
+    # metric: euclidean | cosine
+    metric: euclidean
+    # scanpy | hnsw (from scvelo)
+    method: scanpy
+
+
+
+#-----------------------------
+# Plot
+#-----------------------------
+plotqc:
+  # grouping var must be a categorical varible, 
+  #  (comma-seprated strings, no spaces)
+  # umaps comparing the integration (one plot per value in the group)
+  # for each batch correction column plus any extras in grouping var
+  grouping_var: dataset,sample_id
+  # what other metrics do you want to plot on each modalities embedding, (one plot per group)
+  # use mod:variable notation, 
+  # any metrics that you want to plot on all modality umaps go under "all"
+  # these can be categorical or numeric
+  all: rep:receptor_subtype
+  rna: rna:total_counts
+  prot: prot:total_counts
+  atac:
+  multimodal: rna:total_counts
+  # if you want to add any additional plots, just remove the log file logs/plot_batch_corrected_umaps.log
+  # and run panpipes integration make plot_umaps
+
+# ----------------
+# Make final object
+# ----------------
+# Final choices: Leave blank until you have reviewed the results from running
+# panpipes integration make full
+# This step will produce a mudata object with one layer per modality with 
+# one correction per modality and one multimodal layer.
+# Choose the integration results you want to merge in the final object
+# For unimodal integration: to pick the uncorrected version use "no_correction"
+# then run
+# panpipes integration make merge_integration
+final_obj:
+  rna:
+    include: True
+    bc_choice: no_correction
+  prot:
+    include: True
+    bc_choice: harmony
+  atac:
+    include: False
+    bc_choice: bbknn
+  multimodal:
+    include: True
+    bc_choice: WNN
+