SRP102259

   Project:  SRP102259
   Organism:  Homo sapiens
   Study Title:  Single-Cell Whole Genome Analyses by Linear Amplification via Transposon Insertion (LIANTI)
   Center Name:  Harvard University
   Description:  Single-cell genomics is important for biology and medicine. However, current whole genome amplification (WGA) methods are limited by low accuracy of copy number variation (CNV) detection and low amplification fidelity. Here we report an improved single-cell WGA method, Linear Amplification via Transposon Insertion (LIANTI), which outperforms existing methods, enabling micro-CNV detection with kilobase resolution. This allowed direct observation of stochastic firing of DNA replication origins, different from cell to cell. We also show that the predominant cytosine-to-thymine mutations observed in single-cell genomics often arise from the artifact of cytosine deamination upon cell lysis. However, calling single nucleotide variations (SNVs) can be accomplished by sequencing kindred cells. We determined the spectrum of SNVs in a single human cell after ultraviolet radiation, revealing their nonrandom genome-wide distribution.
   Cell Type:  notcancer-fibroblast
   Median Sequencing Depth:  21.268686
   Publication:  Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI)
   DOI:  10.1126/science.aak9787