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Atlas-scale single-cell chromatin accessibility using nanowell-based combinatorial indexing.
O'Connell, Brendan L; Nichols, Ruth V; Pokholok, Dmitry; Thomas, Jerushah; Acharya, Sonia N; Nishida, Andrew; Thornton, Casey A; Co, Marissa; Fields, Andrew J; Steemers, Frank J; Adey, Andrew C.
Afiliação
  • O'Connell BL; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Nichols RV; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Pokholok D; ScaleBio, San Diego, California 92121, USA.
  • Thomas J; ScaleBio, San Diego, California 92121, USA.
  • Acharya SN; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Nishida A; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Thornton CA; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Co M; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Fields AJ; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA.
  • Steemers FJ; ScaleBio, San Diego, California 92121, USA.
  • Adey AC; Oregon Health & Science University, Department of Molecular and Medical Genetics, Portland, Oregon 97239, USA; adey@ohsu.edu.
Genome Res ; 33(2): 208-217, 2023 02.
Article em En | MEDLINE | ID: mdl-36792372
ABSTRACT
Here we present advancements in single-cell combinatorial indexed Assay for Transposase Accessible Chromatin (sciATAC) to measure chromatin accessibility that leverage nanowell chips to achieve atlas-scale cell throughput (>105 cells) at low cost. The platform leverages the core of the sciATAC workflow where multiple indexed tagmentation reactions are performed, followed by pooling and distribution to a second set of reaction wells for polymerase chain reaction (PCR)-based indexing. In this work, we instead leverage a chip containing 5184 nanowells at the PCR stage of indexing, enabling a 52-fold improvement in scale and reduction in per-cell preparation costs. We detail three variants that balance cell throughput and depth of coverage, and apply these methods to banked mouse brain tissue, producing maps of cell types as well as neuronal subtypes that include integration with existing single-cell Assay for Transposase Accessible Chromatin (scATAC) and scRNA-seq data sets. Our optimized workflow achieves a high fraction of reads that fall within called peaks (>80%) and low cell doublet rates. The high cell coverage technique produces high unique reads per cell, while retaining high enrichment for open chromatin regions, enabling the assessment of >70,000 unique accessible loci on average for each cell profiled. When compared to current methods in the field, our technique provides similar or superior per-cell information with very low levels of cell-to-cell cross talk, and achieves this at a cost point much lower than existing assays.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromatina / Transposases Limite: Animals Idioma: En Revista: Genome Res Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromatina / Transposases Limite: Animals Idioma: En Revista: Genome Res Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos