Chen-Shan Chin
Molecular Biology · 2010–2019
A researcher in the Science corpus: 10 papers; trusts 3 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 166 citations into it; #5,265 of 17,773 by trust here, #2,009 by citations
- Genetics — 81 citations into it
- Ecology — 18 citations into it; #4,462 of 10,717 by trust here, #1,960 by citations
Whom Chen-Shan Chin trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Mark J. P. Chaisson
- Felipe A. Simão
- Christopher J. Lee
- Glenn Tesler
- Daniel D. Sommer
- Eugene W. Myers
- Arthur L. Delcher
- Stefan Kurtz
- Sergey Koren
- Adam M. Phillippy
Who trusts Chen-Shan Chin overall
- Sergey Koren
- Heng Li
- Brian Walenz
- Arang Rhie
- Mikhail Kolmogorov
- Yu Lin
- Robert Vaser
- Jeffrey Yuan
- Anthony Rhoads
- Marten Boetzer
Papers from Chen-Shan Chin's perspective
Ordered by how strongly the researchers Chen-Shan Chin trusts endorse each paper. Same corpus, a different order for every researcher.
- Identification of common molecular subsequences.
- The fragment assembly string graph (ECCB/JBI)
- Real-Time DNA Sequencing from Single Polymerase Molecules (Science)
- Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
- Limitations of next-generation genome sequence assembly (Nature Methods)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- A universal SNP and small-indel variant caller using deep neural networks
- A synthetic-diploid benchmark for accurate variant calling evaluation
- Minimus: a fast, lightweight genome assembler (BMC Bioinformatics)
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
Their papers
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (2014) — 901 citations
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- Phased Diploid Genome Assembly with Single Molecule Real-Time Sequencing (2016) — 1,743 citations
- Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data (2013) — 3,955 citations
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly (2016) — 1,005 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- The Origin of the Haitian Cholera Outbreak Strain (2010) — 723 citations
- Improved maize reference genome with single-molecule technologies (2017) — 1,069 citations
- Validation of ITD mutations in FLT3 as a therapeutic target in human acute myeloid leukaemia (2012) — 732 citations
- Origins of the E. coli Strain Causing an Outbreak of Hemolytic–Uremic Syndrome in Germany (2011) — 862 citations