Han Xu
Molecular Biology · Nature Genetics · 2012–2015
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 103 citations into it
- Genetics — 86 citations into it
Whom Han Xu trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Han Xu's perspective
Ordered by how strongly the researchers Han Xu trusts endorse each paper. Same corpus, a different order for every researcher.
- Controlling the false discovery rate: a practical and powerful approach to multiple testing
- RNA-Guided Human Genome Engineering via Cas9
- edgeR: a Bioconductor package for differential expression analysis of digital gene expression data (Bioinform.)
- Normalization of RNA-seq data using factor analysis of control genes or samples (Nature Biotechnology)
- Genetic Screens in Human Cells Using the CRISPR-Cas9 System (Science)
- baySeq: Empirical Bayesian methods for identifying differential expression in sequence count data (BMC Bioinformatics)
- Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
- High frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells
- A probability-based approach for the analysis of large-scale RNAi screens (Nature Methods)
- High-throughput screening of a CRISPR/Cas9 library for functional genomics in human cells (Nature)
Their papers
- Partitioning heritability by functional annotation using genome-wide association summary statistics (2015) — 2,445 citations
- MAGeCK enables robust identification of essential genes from genome-scale CRISPR/Cas9 knockout screens (2014) — 2,340 citations
- Chromatin marks identify critical cell types for fine mapping complex trait variants (2012) — 604 citations
- EZH2 Oncogenic Activity in Castration Resistant Prostate Cancer Cells is Polycomb-Independent (2012) — 852 citations
- Quality control, modeling, and visualization of CRISPR screens with MAGeCK-VISPR (2015) — 422 citations
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (2014) — 595 citations