Chao Xie
Molecular Biology · 2009–2017
A researcher in the Science corpus: 3 papers; trusts 5 researchers and is trusted by 26 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 21 citations into it; #1,945 of 17,773 by trust here, #4,241 by citations
- Genetics — 12 citations into it
- Ecology — 5 citations into it
Whom Chao Xie trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- W. James Kent
- Ali Mortazavi
- B. Ewing
- John C. Marioni
- Shawn Cokus
- Stephan C. Schuster
- LaDeana W. Hillier
- Christopher E. Mason
- Barbara J. Wold
- Zhong Wang
Who trusts Chao Xie overall
- Martin Steinegger
- Florian P. Breitwieser
- Min Zhao
- Günter Klambauer
- Kai Blin
- Jie Jessie Ren
- Tomás Bruna
- Richa Bharti
- Javier Tamames
- Johannes Söding
Papers from Chao Xie's perspective
Ordered by how strongly the researchers Chao Xie trusts endorse each paper. Same corpus, a different order for every researcher.
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Genome-Wide Mapping of in Vivo Protein-DNA Interactions (Science)
- Detection of large-scale variation in the human genome (Nature Genetics)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning (Nature)
- RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (Genome Research)
- The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing (Science)
- The complete genome of an individual by massively parallel DNA sequencing (Nature)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- Dynamic repertoire of a eukaryotic transcriptome surveyed at single-nucleotide resolution (Nature)
Their papers
- Fast and sensitive protein alignment using DIAMOND (2014) — 11,765 citations
- CNV-seq, a new method to detect copy number variation using high-throughput sequencing (2009) — 573 citations
- No major flaws in “Identification of individuals by trait prediction using whole-genome sequencing data” (2017) — 112 citations