High-throughput single-cell whole-genome amplification through centrifugal emulsification and eMDA

Single-cell whole-genome sequencing (scWGS) is mainly used to probe intercellular genomic variations, focusing on the copy number variations or alterations and the single-nucleotide variations (SNVs) occurring within single cells. Single-cell whole-genome amplification (scWGA) needs to be applied before scWGS but is challenging due to the low copy number of DNA. Besides, many genomic variations are rare within a population of cells, so the throughput of currently available scWGA methods is far from satisfactory. Here, we integrate a one-step micro-capillary array (MiCA)-based centrifugal droplet generation technique with emulsion multiple displacement amplification (eMDA) and demonstrate a high-throughput scWGA method, MiCA-eMDA. MiCA-eMDA increases the single-run throughput of scWGA to a few dozen, and enables the assessment of copy number variations and alterations at 50-kb resolution. Downstream target enrichment further enables the detection of SNVs with 20% allele drop-out.Yusi Fu, Fangli Zhang et al. integrate a one-step microcapillary array with emulsion multiple displacement amplification to obtain a high-throughput single-cell whole-genome amplification method. Their method enables copy number assessment at a resolution of 50 kb.

[1]  Sijia Lu,et al.  Uniform and accurate single-cell sequencing based on emulsion whole-genome amplification , 2015, Proceedings of the National Academy of Sciences.

[2]  F. Tang,et al.  Single-cell multi-omics sequencing of mouse early embryos and embryonic stem cells , 2017, Cell Research.

[3]  Mariella G. Filbin,et al.  Single-cell RNA-seq supports a developmental hierarchy in human oligodendroglioma , 2016, Nature.

[4]  N. Navin Cancer genomics: one cell at a time , 2014, Genome Biology.

[5]  Fangli Zhang,et al.  Centrifugal micro-channel array droplet generation for highly parallel digital PCR. , 2017, Lab on a chip.

[6]  Richard Durbin,et al.  Fast and accurate long-read alignment with Burrows–Wheeler transform , 2010, Bioinform..

[7]  X. Xie,et al.  Genome-Wide Detection of Single-Nucleotide and Copy-Number Variations of a Single Human Cell , 2012, Science.

[8]  Charles Gawad,et al.  A Quantitative Comparison of Single-Cell Whole Genome Amplification Methods , 2014, PloS one.

[9]  F. Dean,et al.  Rapid amplification of plasmid and phage DNA using Phi 29 DNA polymerase and multiply-primed rolling circle amplification. , 2001, Genome research.

[10]  M. DePristo,et al.  The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.

[11]  W. Koh,et al.  Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics , 2014, Proceedings of the National Academy of Sciences.

[12]  S. Horvath,et al.  Genetic programs in human and mouse early embryos revealed by single-cell RNA sequencing , 2013, Nature.

[13]  Hannah A. Pliner,et al.  The cis-regulatory dynamics of embryonic development at single cell resolution , 2017, Nature.

[14]  N. Neff,et al.  Reconstructing lineage hierarchies of the distal lung epithelium using single cell RNA-seq , 2014, Nature.

[15]  I. Amit,et al.  Massively Parallel Single-Cell RNA-Seq for Marker-Free Decomposition of Tissues into Cell Types , 2014, Science.

[16]  Richard Durbin,et al.  Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .

[17]  F. Tang,et al.  Single-cell methylome landscapes of mouse embryonic stem cells and early embryos analyzed using reduced representation bisulfite sequencing , 2013, Genome research.

[18]  E. Shapiro,et al.  Single-cell sequencing-based technologies will revolutionize whole-organism science , 2013, Nature Reviews Genetics.

[19]  C. Ponting,et al.  G&T-seq: parallel sequencing of single-cell genomes and transcriptomes , 2015, Nature Methods.

[20]  Howard Y. Chang,et al.  Single-cell chromatin accessibility reveals principles of regulatory variation , 2015, Nature.

[21]  Andrew C. Adey,et al.  Sequencing thousands of single-cell genomes with combinatorial indexing , 2017, Nature Methods.

[22]  R. Sandberg,et al.  Single-Cell RNA-Seq Reveals Dynamic, Random Monoallelic Gene Expression in Mammalian Cells , 2014, Science.

[23]  Nathan C. Sheffield,et al.  Single-Cell DNA Methylome Sequencing and Bioinformatic Inference of Epigenomic Cell-State Dynamics , 2015, Cell reports.

[24]  Eric J. Alm,et al.  Virtual Microfluidics for digital quantification and single-cell sequencing , 2016, Nature Methods.

[25]  X. Xie,et al.  Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients , 2013, Proceedings of the National Academy of Sciences.

[26]  N. Carter,et al.  Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. , 1992, Genomics.

[27]  Fangli Zhang,et al.  Spinning micropipette liquid emulsion generator for single cell whole genome amplification. , 2016, Lab on a chip.

[28]  Tal Nawy,et al.  Single-cell sequencing , 2013, Nature Methods.

[29]  Charles H. Yoon,et al.  Dissecting the multicellular ecosystem of metastatic melanoma by single-cell RNA-seq , 2016, Science.

[30]  J. Troge,et al.  Tumour evolution inferred by single-cell sequencing , 2011, Nature.

[31]  Annapurna Poduri,et al.  Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain , 2014, Cell reports.

[32]  Lu Wen,et al.  Single-cell triple omics sequencing reveals genetic, epigenetic, and transcriptomic heterogeneity in hepatocellular carcinomas , 2016, Cell Research.

[33]  N. Navin,et al.  Clonal Evolution in Breast Cancer Revealed by Single Nucleus Genome Sequencing , 2014, Nature.

[34]  Ira M. Hall,et al.  Mosaic Copy Number Variation in Human Neurons , 2013, Science.

[35]  X. Xie,et al.  Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI) , 2017, Science.

[36]  Michael Wigler,et al.  Genome-wide copy number analysis of single cells , 2012, Nature Protocols.

[37]  Kun Zhang,et al.  Massively parallel polymerase cloning and genome sequencing of single cells using nanoliter microwells , 2013, Nature Biotechnology.

[38]  Steven L Salzberg,et al.  Fast gapped-read alignment with Bowtie 2 , 2012, Nature Methods.

[39]  Mikael Huss,et al.  Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst. , 2010, Developmental cell.