作者
Lukas Heumos,Anna C. Schaar,Christopher Lance,Anastasia Litinetskaya,Felix Drost,Luke Zappia,Malte Lücken,Daniel Strobl,Juan D. Henao,Fabiola Curion,Hananeh Aliee,Meshal Ansari,Pau Badia-i-Mompel,Maren Büttner,Emma Dann,Daniel Dimitrov,Leander Dony,Amit Frishberg,Dongze He,Soroor Hediyeh-zadeh,Leon Hetzel,Ignacio L. Ibarra,Matthew G. Jones,Mohammad Lotfollahi,Laura D. Martens,Christian L. Müller,Mor Nitzan,Johannes Ostner,Giovanni Palla,Rob Patro,Zoe Piran,Ciro Ramírez-Suástegui,Julio Sáez-Rodríguez,Hirak Sarkar,Benjamin Schubert,Lisa Sikkema,Avi Srivastava,Jovan Tanevski,Isaac Virshup,Philipp Weiler,Herbert B. Schiller,Fabian J. Theis
摘要
Recent advances in single-cell technologies have enabled high-throughput molecular profiling of cells across modalities and locations. Single-cell transcriptomics data can now be complemented by chromatin accessibility, surface protein expression, adaptive immune receptor repertoire profiling and spatial information. The increasing availability of single-cell data across modalities has motivated the development of novel computational methods to help analysts derive biological insights. As the field grows, it becomes increasingly difficult to navigate the vast landscape of tools and analysis steps. Here, we summarize independent benchmarking studies of unimodal and multimodal single-cell analysis across modalities to suggest comprehensive best-practice workflows for the most common analysis steps. Where independent benchmarks are not available, we review and contrast popular methods. Our article serves as an entry point for novices in the field of single-cell (multi-)omic analysis and guides advanced users to the most recent best practices.