Zhouzhi Wang
Genetics · 2006–2016
A researcher in the Science corpus: 5 papers; trusts 13 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 73 citations into it
- Molecular Biology — 49 citations into it; #5,381 of 17,773 by trust here, #3,803 by citations
- Computational Biology & Bioinformatics — 12 citations into it
Whom Zhouzhi Wang trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Robert C. Edgar
- Julie Dawn Thompson
- Kazutaka Katoh
- Temple F. Smith
- Timo Lassmann
- Christopher Sander
- Christopher J. Lee
- Chuong B. Do
- K. Kuma
Who trusts Zhouzhi Wang overall
Papers from Zhouzhi Wang's perspective
Ordered by how strongly the researchers Zhouzhi Wang trusts endorse each paper. Same corpus, a different order for every researcher.
- MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform.
- The Pfam protein families database
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.
- Identification of common molecular subsequences.
- MUSCLE: a multiple sequence alignment method with reduced time and space complexity
- Multiple sequence alignment using partial order graphs
- Kalign – an accurate and fast multiple sequence alignment algorithm (BMC Bioinformatics)
- MAFFT version 5: improvement in accuracy of multiple sequence alignment
- ProbCons: Probabilistic consistency-based multiple sequence alignment. (Genome Research)
- Database of homology‐derived protein structures and the structural meaning of sequence alignment
Their papers
- The accuracy of several multiple sequence alignment programs for proteins (2006) — 372 citations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects (2016) — 996 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations