Zemin Ning
Molecular Biology · 2001–2020
A researcher in the Science corpus: 15 papers; trusts 22 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 313 citations into it; #3,120 of 17,773 by trust here, #270 by citations
- Genetics — 144 citations into it; #5,553 of 6,854 by trust here, #60 by citations
- Plant Science — 101 citations into it
- Ecology — 39 citations into it
- Computational Biology & Bioinformatics — 20 citations into it
- Biomedical Engineering — 7 citations into it
Whom Zemin Ning trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Donald Ervin Knuth
- Stephen F. Altschul
- Temple F. Smith
- Zheng Zhang
- Nicholas J. Loman
- David Altshuler
- Mihai Pop
- Heng Li
- Mark J. P. Chaisson
- Michael S. Waterman
Who trusts Zemin Ning overall
- Heng Li
- Jay Shendure
- Robert Schmieder
- Shivashankar H. Nagaraj
- Arthur L. Delcher
- Nils Homer
- Ying Chen
- Peter J. A. Cock
- Michael Roberts
- Sergey Koren
Papers from Zemin Ning's perspective
Ordered by how strongly the researchers Zemin Ning trusts endorse each paper. Same corpus, a different order for every researcher.
- Basic local alignment search tool.
- Identification of common molecular subsequences.
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (Nature Biotechnology)
- Hybrid error correction and de novo assembly of single-molecule sequencing reads (Nature Biotechnology)
- Limitations of next-generation genome sequence assembly (Nature Methods)
- A Greedy Algorithm for Aligning DNA Sequences (J. Comput. Biol.)
- De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer. (Genome Research)
- Multiple sequence alignment using partial order graphs
- SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing (J. Comput. Biol.)
Their papers
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (2008) — 3,840 citations
- SSAHA: a fast search method for large DNA databases. (2001) — 1,044 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Assemblathon 1: a competitive assessment of de novo short read assembly methods. (2011) — 544 citations
- Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads (2009) — 2,074 citations
- Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations
- Towards complete and error-free genome assemblies of all vertebrate species (2020) — 2,673 citations
- A comprehensive catalogue of somatic mutations from a human cancer genome (2009) — 1,716 citations
- International network of cancer genome projects (2010) — 2,229 citations
- Insights into hominid evolution from the gorilla genome sequence (2012) — 719 citations
- Oxford Nanopore MinION Sequencing and Genome Assembly (2016) — 765 citations
- The zebrafish reference genome sequence and its relationship to the human genome (2013) — 4,740 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- The Schistosoma japonicum genome reveals features of host-parasite interplay (2009) — 648 citations
- The genome of the blood fluke Schistosoma mansoni (2009) — 1,033 citations