Andrew Whitwham
Genetics · 2020–2021
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 22 citations into it
Whom Andrew Whitwham trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li (in Genetics)
Papers from Andrew Whitwham's perspective
Ordered by how strongly the researchers Andrew Whitwham trusts endorse each paper. Same corpus, a different order for every researcher.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- The Ensembl Variant Effect Predictor
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- AddressSanitizer: A Fast Address Sanity Checker
- BCFtools/RoH: a hidden Markov model approach for detecting autozygosity from next-generation sequencing data (Bioinform.)
- Improving SNP discovery by base alignment quality (Bioinform.)
- JBrowse: a dynamic web platform for genome visualization and analysis (Genome Biology)
- Bioconda: sustainable and comprehensive software distribution for the life sciences (Nature Methods)
- The human genome browser at UCSC.
Their papers
- Twelve years of SAMtools and BCFtools (2020) — 12,495 citations
- HTSlib: C library for reading/writing high-throughput sequencing data (2021) — 332 citations
- Hospital admission and emergency care attendance risk for SARS-CoV-2 delta (B.1.617.2) compared with alpha (B.1.1.7) variants of concern: a cohort study (2021) — 720 citations
- Assessing transmissibility of SARS-CoV-2 lineage B.1.1.7 in England (2021) — 1,098 citations
- SARS-CoV-2 evolution during treatment of chronic infection (2021) — 955 citations