Charles Markello
Molecular Biology · 2018–2022
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 — 83 citations into it
- Genetics — 51 citations into it
Whom Charles Markello trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Charles Markello's perspective
Ordered by how strongly the researchers Charles Markello trusts endorse each paper. Same corpus, a different order for every researcher.
- 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)
- A universal SNP and small-indel variant caller using deep neural networks
- Additional file 6
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Multiple sequence alignment using partial order graphs
- Reducing storage requirements for biological sequence comparison (Bioinform.)
- The design and construction of reference pangenome graphs with minigraph (Genome Biology)
- A global reference for human genetic variation
Their papers
- Variation graph toolkit improves read mapping by representing genetic variation in the reference (2018) — 681 citations
- Pangenomics enables genotyping known structural variants in 5,202 diverse genomes (2021) — 309 citations
- A draft human pangenome reference (2022) — 882 citations