Nadia Pisanti
Genetics · 2015–2016
A researcher in the Science corpus: 2 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 19 citations into it
- Molecular Biology — 18 citations into it
Whom Nadia Pisanti trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Nadia Pisanti's perspective
Ordered by how strongly the researchers Nadia Pisanti trusts endorse each paper. Same corpus, a different order for every researcher.
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- Haplotype phasing: Existing methods and new developments (Nature reviews genetics)
- Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data. (Genetics)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- A linear complexity phasing method for thousands of genomes (Nature Methods)
- A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies (PLoS Genetics)
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
Their papers
- WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads (2015) — 410 citations
- WhatsHap: fast and accurate read-based phasing (2016) — 406 citations