Evan E. Eichler
Molecular Biology · 2001–2023
A researcher in the Science corpus: 62 papers; trusts 18 researchers and is trusted by 12 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 881 citations into it; #3,955 of 17,773 by trust here, #57 by citations
- Genetics — 719 citations into it; #1,585 of 6,854 by trust here, #19 by citations
- Plant Science — 352 citations into it; #5,054 of 8,232 by trust here, #72 by citations
- Artificial Intelligence — 56 citations into it
- Ecology — 54 citations into it
Whom Evan E. Eichler trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Elaine R. Mardis
- Jonathan C. Cohen
- Mark J. P. Chaisson
- Heather J. Cordell
- P. Phillips
- Ryan R. Wick
Who trusts Evan E. Eichler overall
- Andreas Wagner
- Jian Yang
- Computational Pan-Genomics Consortium
- Todd J. Treangen
- Heng Li
- Greg Gibson
- Min Zhao
Papers from Evan E. Eichler's perspective
Ordered by how strongly the researchers Evan E. Eichler trusts endorse each paper. Same corpus, a different order for every researcher.
- An Eulerian path approach to DNA fragment assembly (Proceedings of the National Academy of Sciences of the United States of America)
- Velvet: algorithms for de novo short read assembly using de Bruijn graphs.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- Real-Time DNA Sequencing from Single Polymerase Molecules (Science)
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (American Journal of Human Genetics)
- Assembling large genomes with single-molecule sequencing and locality-sensitive hashing (Nature Biotechnology)
- The fragment assembly string graph (ECCB/JBI)
- Common deletion polymorphisms in the human genome (Nature Genetics)
- Exome sequencing as a tool for Mendelian disease gene discovery
Their papers
- Initial sequencing and analysis of the human genome (2001) — 24,262 citations
- Resolving the complexity of the human genome using single-molecule sequencing (2014) — 769 citations
- Limitations of next-generation genome sequence assembly (2010) — 742 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Segmental duplications: organization and impact within the current human genome project assembly. (2001) — 709 citations
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) — 2,140 citations
- Initial sequence of the chimpanzee genome and comparison with the human genome (2005) — 2,343 citations
- Diversity of Human Copy Number Variation and Multicopy Genes (2010) — 724 citations
- HiCanu: accurate assembly of segmental duplications, satellites, and allelic variants from high-fidelity long reads (2020) — 634 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
- Segmental duplications and copy-number variation in the human genome. (2005) — 993 citations
- Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
- Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution (2004) — 2,677 citations
- Genome structural variation discovery and genotyping (2011) — 1,575 citations
- Tumour invasion and metastasis initiated by microRNA-10b in breast cancer (2008) — 1,058 citations
- Recent Segmental Duplications in the Human Genome (2002) — 1,428 citations
- The Human Pangenome Project: a global resource to map genomic diversity (2022) — 392 citations
- Long-read human genome sequencing and its applications (2020) — 944 citations