Haley Abel
Molecular Biology · 2016–2022
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 106 citations into it
- Genetics — 99 citations into it
Whom Haley Abel trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Haley Abel overall
Papers from Haley Abel's perspective
Ordered by how strongly the researchers Haley Abel trusts endorse each paper. Same corpus, a different order for every researcher.
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- The Ensembl Variant Effect Predictor
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (American Journal of Human Genetics)
- A universal SNP and small-indel variant caller using deep neural networks
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
- Mapping copy number variation by population scale genome sequencing (Nature)
- Additional file 6
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies (Genome Biology)
Their papers
- High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios (2021) — 932 citations
- SVScore: an impact prediction tool for structural variation (2016) — 52 citations
- A draft human pangenome reference (2022) — 882 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations