V. Ohan
Genetics · 2020–2021
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
- Genetics — 20 citations into it
Whom V. Ohan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from V. Ohan's perspective
Ordered by how strongly the researchers V. Ohan 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 Ensembl Variant Effect Predictor
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- Bioconda: sustainable and comprehensive software distribution for the life sciences (Nature Methods)
- 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)
- Exome sequencing as a tool for Mendelian disease gene discovery
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
- SARS-CoV-2 evolution during treatment of chronic infection (2021) — 955 citations