HIPSD&R-seq enables scalable genomic copy number and transcriptome profiling.

HIPSD&R-seq 可实现可扩展的基因组拷贝数和转录组分析

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作者:Otoničar Jan, Lazareva Olga, Mallm Jan-Philipp, Simovic-Lorenz Milena, Philippos George, Sant Pooja, Parekh Urja, Hammann Linda, Li Albert, Yildiz Umut, Marttinen Mikael, Zaugg Judith, Noh Kyung Min, Stegle Oliver, Ernst Aurélie
Single-cell DNA sequencing (scDNA-seq) enables decoding somatic cancer variation. Existing methods are hampered by low throughput or cannot be combined with transcriptome sequencing in the same cell. We propose HIPSD&R-seq (HIgh-throughPut Single-cell Dna and Rna-seq), a scalable yet simple and accessible assay to profile low-coverage DNA and RNA in thousands of cells in parallel. Our approach builds on a modification of the 10X Genomics platform for scATAC and multiome profiling. In applications to human cell models and primary tissue, we demonstrate the feasibility to detect rare clones and we combine the assay with combinatorial indexing to profile over 17,000 cells.

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