DLP+ Single Cell Whole Genome Sequencing

DLP+ is a high-throughput direct transposition single-cell whole-genome sequencing approach, based on commodity high-density nanowell arrays and picoliter-volume piezo-dispensing technology available “off the shelf”. DLP+ permits cost-effective shallow sequencing of thousands of cells, rather than sequencing fewer cells at greater depth. DLP+ data can be used to identify clonal populations and their genomic features, properties of individual cells including replication state and chromosomal mis-segregation, and relationships between genomic and morphological properties.

About the Data Data Levels Data Access

About the Data

Method and Protocol

Learn about this method and protocol in Laks, McPherson, et al. Cell (2019). DOI:10.1016/j.cell.2019.10.026

Data Visualization

An HTML report with preliminary analysis is available to explore. See Data Access and Visualization, below

Data Access

Access the data through:

  • Level 1: FASTQ (By request with DUA)
  • Level 2: BAM (EGA)
  • Level 3: CSV, HTML (AWS)

For a description of the files see the table below.

About the Samples

The following are planned to be sequenced:

  • 100 breast samples

Instruments

DLP+ uses a contactless piezoelectric dispensing platform, such as the sciFLEXARRAYER S3 or cellenONE

Reactions are carried out on a high-density nanowell chip, in this case a WaferGen (SmartChip) array

For more information, see Instrument Information (below)

About the Data Generators

This data was generated and analyzed in the lab of Sam Aparicio.


Data Levels:

Data Level Description File Format File Size (per sample) Data Access
Raw sequences (Level 1) Nucleotide sequence and quality scores FASTQ   By request with DUA
Aligned sequences (Level 2) Sequencing data aligned to a reference genome BAM   EGA
Aggregated data (Level 3) QC, analysis, and exploration of sequencing data CSV, HTML   AWS
All files Total per sample   130 GB  


Instrument Information

DLP+ uses a contactless piezoelectric dispensing platform to deposit single cells and reagents as picoliter-scale droplets into an open nanowell array, using commercially available instruments such as the sciFLEXARRAYER S3 or cellenONE. Reactions are carried out on a high-density nanowell chip, in this case a WaferGen (SmartChip) array, which serves as the physical substrate for parallelized single-cell library construction. The dispensing setup incorporates integrated imaging, including droplet and nozzle cameras, enabling image-based selection and quality control to avoid depositing doublets or debris. The spotter workstation also includes practical peripherals such as a chilled chip holder or target stage, a wash-solution reservoir, and an active wash station to support reliable dispensing and minimize carryover between deposits.

Data Access and Visualization

Several levels of primary and processed data are available via the data cards below:

  1. A summary report showing basic quality control and a preliminary analysis of the data.
  2. Processed CNA data including all single-cell copy number calls.
  3. Primary sequencing data available from the European Genome-Phenome Archive (EGA). A Data Access Agreement between your institution and EGA will be required.
Summary Report: Single-Cell Copy Number Alteration Overview
Processed CNA Data: Single-Cell Copy Number Calls
Primary Sequencing Data: DLP+ Single-Cell Whole Genome Sequencing of Luminal Breast Epithelial Cells from Wildtype and BRCA Mutation Carriers