John Marshall
Genetics · with Bonfield · 2020–2021
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 15 citations into it
Whom John Marshall trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts John Marshall overall
Papers from John Marshall's perspective
Ordered by how strongly the researchers John Marshall 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.)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- The Ensembl Variant Effect Predictor
- Bioconda: sustainable and comprehensive software distribution for the life sciences (Nature Methods)
- 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)
- 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