J. Monlong
Molecular Biology · 2020–2022
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 107 citations into it
Whom J. Monlong trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from J. Monlong's perspective
Ordered by how strongly the researchers J. Monlong trusts endorse each paper. Same corpus, a different order for every researcher.
- A universal SNP and small-indel variant caller using deep neural networks
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (Nature Biotechnology)
- Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies (Genome Biology)
- Limitations of next-generation genome sequence assembly (Nature Methods)
- Additional file 6
- Reducing storage requirements for biological sequence comparison (Bioinform.)
- On the resemblance and containment of documents
- The design and construction of reference pangenome graphs with minigraph (Genome Biology)
- An integrated map of structural variation in 2,504 human genomes (Nature)
- A global reference for human genetic variation
Their papers
- Pangenomics enables genotyping known structural variants in 5,202 diverse genomes (2021) — 309 citations
- Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes (2020) — 428 citations
- A draft human pangenome reference (2022) — 882 citations