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Open AccessSimultaneous de novo calling and phasing of genetic variants at chromosome-scale using NanoStrand-seq
The successful accomplishment of the first telomere-to-telomere human genome assembly, T2T-CHM13, marked a milestone in achieving completeness of the human reference genome. The upcoming era of genome study wi...
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Article
Open AccessUnveiling gene regulatory networks during cellular state transitions without linkage across time points
Time-stamped cross-sectional data, which lack linkage across time points, are commonly generated in single-cell transcriptional profiling. Many previous methods for inferring gene regulatory networks (GRNs) dr...
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Article
Open AccessDEAD-box helicase 17 (DDX17) protects cardiac function by promoting mitochondrial homeostasis in heart failure
DEAD-box helicase 17 (DDX17) is a typical member of the DEAD-box family with transcriptional cofactor activity. Although DDX17 is abundantly expressed in the myocardium, its role in heart is not fully understo...
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Article
Open AccessMap** crossover events of mouse meiotic recombination by restriction fragment ligation-based Refresh-seq
Single-cell whole-genome sequencing methods have undergone great improvements over the past decade. However, allele dropout, which means the inability to detect both alleles simultaneously in an individual dip...
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Article
Blastoids generated purely from embryonic stem cells both in mice and humans
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scNanoCOOL-seq: a long-read single-cell sequencing method for multi-omics profiling within individual cells
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scNanoHi-C: a single-cell long-read concatemer sequencing method to reveal high-order chromatin structures within individual cells
The high-order three-dimensional (3D) organization of regulatory genomic elements provides a topological basis for gene regulation, but it remains unclear how multiple regulatory elements across the mammalian ...
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Author Correction: In vitro expansion of human sperm through nuclear transfer
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Open AccessBase editing-mediated one-step inactivation of the Dnmt gene family reveals critical roles of DNA methylation during mouse gastrulation
During embryo development, DNA methylation is established by DNMT3A/3B and subsequently maintained by DNMT1. While much research has been done in this field, the functional significance of DNA methylation in e...
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Article
Temporal and spatial stability of the EM/PM molecular subtypes in adult diffuse glioma
Detailed characterizations of genomic alterations have not identified subtype-specific vulnerabilities in adult gliomas. Map** gliomas into developmental programs may uncover new vulnerabilities that are not...
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Open AccessCharacterization of mesenchymal stem cells in human fetal bone marrow by single-cell transcriptomic and functional analysis
Bone marrow mesenchymal stromal/stem cells (MSCs) are a heterogeneous population that can self-renew and generate stroma, cartilage, fat, and bone. Although a significant progress has been made toward recogniz...
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Open AccessPublisher Correction: High-throughput and high-sensitivity full-length single-cell RNA-seq analysis on third-generation sequencing platform
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Open AccessRelationships of tumor differentiation and immune infiltration in gastric cancers revealed by single-cell RNA-seq analyses
Gastric cancers are highly heterogeneous malignant tumors. To reveal the relationship between differentiation status of cancer cells and tumor immune microenvironments in gastric cancer, single-cell RNA-sequen...
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Open AccessHigh-throughput and high-sensitivity full-length single-cell RNA-seq analysis on third-generation sequencing platform
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Open AccessscNanoATAC-seq: a long-read single-cell ATAC sequencing method to detect chromatin accessibility and genetic variants simultaneously within an individual cell
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Open AccessSingle-cell transcriptomic profiling reveals the tumor heterogeneity of small-cell lung cancer
Small-cell lung cancer (SCLC) is the most aggressive and lethal subtype of lung cancer, for which, better understandings of its biology are urgently needed. Single-cell sequencing technologies provide an oppor...
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Open AccessSingle-cell profiling reveals molecular basis of malignant phenotypes and tumor microenvironments in small bowel adenocarcinomas
Small bowel adenocarcinomas (SBAs) are rare malignant tumors with a high mortality rate, and their molecular characteristics are still largely unexplored. Here we performed single-cell RNA sequencing for tumor...
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Open AccessSingle-cell genomic and transcriptomic landscapes of primary and metastatic colorectal cancer tumors
Colorectal cancer (CRC) ranks as the second-leading cause of cancer-related death worldwide with metastases being the main cause of cancer-related death. Here, we investigated the genomic and transcriptomic al...
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Open AccessMolecular profiling of human non-small cell lung cancer by single-cell RNA-seq
Lung cancer, one of the most common malignant tumors, exhibits high inter- and intra-tumor heterogeneity which contributes significantly to treatment resistance and failure. Single-cell RNA sequencing (scRNA-s...
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Open AccessSystematic evaluation of colorectal cancer organoid system by single-cell RNA-Seq analysis
Patient-derived organoid culture is a powerful system for studying the molecular mechanisms of cancers, especially colorectal cancer (CRC), one of the most prevalent cancers worldwide. There are two main types...