Single Cell or Single Clone Analysis workflows are useful for anyone who is expecting to find one (or more) dominant heavy and light chains in each of their samples. This could be barcoded data where each barcode corresponds to a dominant heavy and light chain pair, or if you have fasta/fastq files where each file is expected to have a dominant chain or pair of chains. This covers a range of different types of experimental processes, including both Single Cell and Single Clone workflows.
Method 1 - Pair, Collapse UMIs, Single Clone Analysis
If you have a fastq/fasta (or other format) file with raw sequences that contain UMI and/or Barcodes and have not been demultiplexed, this is the method to use. The NGS Tutorials 3 & 4 on our website actually follow a similar workflow, so that may be a good place to start. You can find them here: NGS Tutorials 3: Using Barcodes and UMIs and Tutorial 4: Single Clone Antibody Analysis. This tutorial has a small sampled dataset, the full dataset can be provided on request.
A typical workflow could look like:
- Set + Merge Paired Reads: feed raw FASTQ files into 'Set and Merge Paired Reads'. You may wish to choose the "Set pairs only" option if your merge rate is low. The UMI/Barcode tool can handle paired unmerged reads.
- UMI Collapse and Separate Barcodes: Feed paired (or merged) reads into 'Collapse UMI duplicates and Separate Barcodes'. The merges all similar sequences with the same UMI and Barcode together. It is useful to leave the Trim UMIs/Barcodes' option off while experimenting, but you will want to have them trimmed off for the next step. The Barcode will be saved on each sequence as metadata.
- Annotation: Feed the (trimmed) generated consensus sequences into 'Single Clone Analysis'. Single Clone Annotator is a variation of Antibody Annotator that attempts to combine related sequences within a barcode so that you can see the dominant clones. You could also use Antibody Annotator if you wish, which will analyse each of the sequences without merging them. Both tools offer clonotype analysis (our "cluster" tables).
Discovery: Alignments can be done directly from the results so that the aligned sequences are annotated. You can choose to align translated regions of interest, with trees.
Export: Extract selected annotate candidate sequences, or export tables, graphs, and images for reporting or record keeping purposes.
Method 2 - Single Clone Analysis from separate lists
If you or your sequence provider have already done some demultiplexing in another tool, you can feed the preprocessed sequences into Geneious Biologics for annotation and analysis. If you have your sequences sorted into sequence lists (such as one fastq file per clone/barcode/well/cell) then you could use these sequences directly with Single Clone Analysis. When you run Single Clone Analysis on multiple files or sequence lists, then it will attempt to find a dominant heavy and light chain for each list. For more information, see the Single Clone Analysis article.
Method 3 - Antibody Annotator + Add Assay Data
If you have already done some demultiplexing in another tool such as Cell Ranger, but don't have them sorted into sequence lists, then you could feed the consensus sequences directly into Antibody Annotator. Antibody Annotator will annotate FR and CDR regions, identify liabilities, variants relative to germline, clonotypes and more. The "Add Assay Data" feature can also be useful to add any coverage or depth information from csv or excel files from your demultiplexing stage.