A multi-center cross-platform single-cell RNA sequencing reference dataset
暂无分享,去创建一个
Wanqiu Chen | Andrew Farmer | Xin Chen | Zhaowei Yang | Yongmei Zhao | Bao Tran | Vyacheslav Furtak | Malcolm Moos | Wenming Xiao | Charles Wang | W. Xiao | A. Farmer | Bao Tran | Charles Wang | Yongmei Zhao | Zhaowei Yang | Wanqiu Chen | V. Furtak | Malcolm Moos | Xin Chen | Wenming Xiao
[1] Kerstin B. Meyer,et al. BBKNN: fast batch alignment of single cell transcriptomes , 2019, Bioinform..
[2] Evan Z. Macosko,et al. Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets , 2015, Cell.
[3] Salah Ayoub,et al. Cell fixation and preservation for droplet-based single-cell transcriptomics , 2017, BMC Biology.
[4] Grace X. Y. Zheng,et al. Massively parallel digital transcriptional profiling of single cells , 2016, Nature Communications.
[5] M. Robinson,et al. A scaling normalization method for differential expression analysis of RNA-seq data , 2010, Genome Biology.
[6] Bonnie Berger,et al. Efficient integration of heterogeneous single-cell transcriptomes using Scanorama , 2019, Nature Biotechnology.
[7] Thomas R. Gingeras,et al. STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..
[8] R. Satija,et al. Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression , 2019, Genome Biology.
[9] Oliver Stegle,et al. Benchmarking Single-Cell RNA Sequencing Protocols for Cell Atlas Projects , 2019, bioRxiv.
[10] R. Satija,et al. Normalization and variance stabilization of single-cell RNA-seq data using regularized negative binomial regression , 2019, Genome Biology.
[11] Laleh Haghverdi,et al. Batch effects in single-cell RNA-sequencing data are corrected by matching mutual nearest neighbors , 2018, Nature Biotechnology.
[12] K. Holt,et al. Performance of neural network basecalling tools for Oxford Nanopore sequencing , 2019, Genome Biology.
[13] T. Hashimshony,et al. CEL-Seq: single-cell RNA-Seq by multiplexed linear amplification. , 2012, Cell reports.
[14] Paul Hoffman,et al. Integrating single-cell transcriptomic data across different conditions, technologies, and species , 2018, Nature Biotechnology.
[15] Åsa K. Björklund,et al. Smart-seq2 for sensitive full-length transcriptome profiling in single cells , 2013, Nature Methods.
[16] Jiacheng Yao,et al. Comparative analysis of droplet-based ultra-high-throughput single-cell RNA-seq systems , 2018, bioRxiv.
[17] Shuqiang Li,et al. CEL-Seq2: sensitive highly-multiplexed single-cell RNA-Seq , 2016, Genome Biology.
[18] Christoph Hafemeister,et al. Comprehensive integration of single cell data , 2018, bioRxiv.
[19] Fan Zhang,et al. Fast, sensitive, and accurate integration of single cell data with Harmony , 2018, bioRxiv.
[20] R. Sandberg,et al. Full-Length mRNA-Seq from single cell levels of RNA and individual circulating tumor cells , 2012, Nature Biotechnology.
[21] Wei Shi,et al. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features , 2013, Bioinform..
[22] S. Dudoit,et al. Normalization of RNA-seq data using factor analysis of control genes or samples , 2014, Nature Biotechnology.
[23] Maithreyan Srinivasan,et al. Nanogrid single-nucleus RNA sequencing reveals phenotypic diversity in breast cancer , 2017, Nature Communications.
[24] A. Heger,et al. UMI-tools: modeling sequencing errors in Unique Molecular Identifiers to improve quantification accuracy , 2016, bioRxiv.
[25] Kok Siong Ang,et al. A benchmark of batch-effect correction methods for single-cell RNA sequencing data , 2020, Genome Biology.
[26] Christoph Ziegenhain,et al. zUMIs - A fast and flexible pipeline to process RNA sequencing data with UMIs , 2017, bioRxiv.
[27] Marcel Martin. Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .
[28] Luke Zappia,et al. Opportunities and challenges in long-read sequencing data analysis , 2020, Genome Biology.
[29] Pak Chung Sham,et al. Linnorm: improved statistical analysis for single cell RNA-seq expression data , 2017, Nucleic acids research.
[30] Björn Usadel,et al. Trimmomatic: a flexible trimmer for Illumina sequence data , 2014, Bioinform..
[31] J. Zook,et al. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls , 2013, Nature Biotechnology.
[32] I. Hellmann,et al. Comparative Analysis of Single-Cell RNA Sequencing Methods , 2016, bioRxiv.
[33] J. Langeveld,et al. KALLISTO: cost effective and integrated optimization of the urban wastewater system Eindhoven , 2012 .
[34] T. Ohshima,et al. Stimulated emission from nitrogen-vacancy centres in diamond , 2016, Nature Communications.
[35] M. Newton,et al. SCnorm: robust normalization of single-cell RNA-seq data , 2017, Nature Methods.
[36] J. Marioni,et al. Pooling across cells to normalize single-cell RNA sequencing data with many zero counts , 2016, Genome Biology.
[37] Colin N. Dewey,et al. RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome , 2011, BMC Bioinformatics.
[38] Luyi Tian,et al. Benchmarking single cell RNA-sequencing analysis pipelines using mixture control experiments , 2019, Nature Methods.
[39] Leland McInnes,et al. UMAP: Uniform Manifold Approximation and Projection for Dimension Reduction , 2018, ArXiv.