Sergey Koren
Molecular Biology · 2008–2023
A researcher in the Science corpus: 25 papers; trusts 49 researchers and is trusted by 39 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 649 citations into it; #938 of 17,773 by trust here, #271 by citations
- Genetics — 225 citations into it
- Plant Science — 208 citations into it; #2,243 of 8,232 by trust here, #386 by citations
- Ecology — 108 citations into it; #1,880 of 10,717 by trust here, #3,198 by citations
- Artificial Intelligence — 62 citations into it
- Computational Biology & Bioinformatics — 32 citations into it
- Food Science — 12 citations into it
- Information Retrieval & Search — 10 citations into it
Whom Sergey Koren trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Chen-Shan Chin
- Mark J. P. Chaisson
- Pavel A. Pevzner
- Eugene W. Myers
- Konstantin Berlin
- Arthur L. Delcher
- Steven L. Salzberg
- Adam M. Phillippy
- Jared T Simpson
Who trusts Sergey Koren overall
- Sergey Nurk
- Brian Walenz
- Anthony Rhoads
- Arang Rhie
- Heng Li
- Kin Fai Au
- Richa Bharti
- Christoph Bleidorn
- Adam M. Phillippy
- Yu Lin
Papers from Sergey Koren's perspective
Ordered by how strongly the researchers Sergey Koren trusts endorse each paper. Same corpus, a different order for every researcher.
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- An Eulerian path approach to DNA fragment assembly (Proceedings of the National Academy of Sciences of the United States of America)
- Basic local alignment search tool.
- A whole-genome assembly of Drosophila. (Science)
- Identification of common molecular subsequences.
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (Nature Biotechnology)
- Real-Time DNA Sequencing from Single Polymerase Molecules (Science)
- The fragment assembly string graph (ECCB/JBI)
- Limitations of next-generation genome sequence assembly (Nature Methods)
- ALLPATHS: de novo assembly of whole-genome shotgun microreads. (Genome Research)
Their papers
- Nanopore sequencing and assembly of a human genome with ultra-long reads (2017) — 1,714 citations
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (2014) — 901 citations
- A framework for human microbiome research (2012) — 2,418 citations
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation (2016) — 6,453 citations
- Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies (2020) — 3,144 citations
- Structure, Function and Diversity of the Healthy Human Microbiome (2012) — 10,771 citations
- Hybrid error correction and de novo assembly of single-molecule sequencing reads (2012) — 1,002 citations
- HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads (2020) — 634 citations
- Mash: fast genome and metagenome distance estimation using MinHash (2015) — 2,878 citations
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly (2016) — 1,005 citations
- Assemblathon 1: a competitive assessment of de novo short read assembly methods. (2011) — 544 citations
- One chromosome, one contig: complete microbial genomes from long-read sequencing and assembly. (2015) — 402 citations
- De novo assembly of haplotype-resolved genomes with trio binning (2018) — 439 citations
- Aggressive assembly of pyrosequencing reads with mates (2008) — 574 citations
- Towards complete and error-free genome assemblies of all vertebrate species (2020) — 2,673 citations
- GAGE: A critical evaluation of genome assemblies and assembly algorithms. (2012) — 354 citations
- Assembly Algorithms for Next-Generation Sequencing Data (2010) — 1,200 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes (2020) — 428 citations