Aaron M. Wenger
Genetics · 2010–2021
A researcher in the Science corpus: 8 papers; trusts 1 researcher and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Genetics — 113 citations into it
- Computational Biology & Bioinformatics — 19 citations into it
Whom Aaron M. Wenger trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Aaron M. Wenger overall
Papers from Aaron M. Wenger's perspective
Ordered by how strongly the researchers Aaron M. Wenger trusts endorse each paper. Same corpus, a different order for every researcher.
- The human genome browser at UCSC.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Real-Time DNA Sequencing from Single Polymerase Molecules (Science)
- A universal SNP and small-indel variant caller using deep neural networks
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
- 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)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
- An integrated semiconductor device enabling non-optical genome sequencing (Nature)
Their papers
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (2019) — 1,512 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- GREAT improves functional interpretation of cis-regulatory regions (2010) — 4,375 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- Variant Review with the Integrative Genomics Viewer (IGV) (2017) — 957 citations
- The complete sequence of a human genome (2021) — 2,469 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations
- M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity (2016) — 797 citations