Jana Ebler
Molecular Biology · 2019–2022
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 — 100 citations into it
Whom Jana Ebler trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Jana Ebler's perspective
Ordered by how strongly the researchers Jana Ebler trusts endorse each paper. Same corpus, a different order for every researcher.
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
- A universal SNP and small-indel variant caller using deep neural networks
- Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies (Genome Biology)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- 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)
- Limitations of next-generation genome sequence assembly (Nature Methods)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Additional file 6
- Multiple sequence alignment using partial order graphs
Their papers
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- A draft human pangenome reference (2022) — 882 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations