Komal Sanjeev
Genetics · 2015
A researcher in the Science corpus: 1 paper; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 18 citations into it
Whom Komal Sanjeev trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Komal Sanjeev's perspective
Ordered by how strongly the researchers Komal Sanjeev 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
- Genotype and SNP calling from next-generation sequencing data (Nature reviews genetics)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Estimating Individual Admixture Proportions from Next Generation Sequencing Data (Genetics)
- PLINK: a tool set for whole-genome association and population-based linkage analyses.
- ml‐relate: a computer program for maximum likelihood estimation of relatedness and relationship
- SNP Calling, Genotype Calling, and Sample Allele Frequency Estimation from New-Generation Sequencing Data (PLoS ONE)
- Ancient Admixture in Human History (Genetics)
- Robust relationship inference in genome-wide association studies
Their papers
- Maximum Likelihood Estimation of Biological Relatedness from Low Coverage Sequencing Data (2015) — 116 citations