Vineet Bafna
Molecular Biology · 2001–2017
A researcher in the Science corpus: 9 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 147 citations into it
- Genetics — 84 citations into it
Whom Vineet Bafna trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Vineet Bafna overall
Papers from Vineet Bafna's perspective
Ordered by how strongly the researchers Vineet Bafna trusts endorse each paper. Same corpus, a different order for every researcher.
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- Alu repeats and human genomic diversity (Nature reviews genetics)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- Exome sequencing as a tool for Mendelian disease gene discovery
- Amino acid substitution matrices from protein blocks.
- The Pfam protein families database
- A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. (Systematic Biology)
- A three-dimensional map of the human genome at kilobase resolution reveals principles of chromatin looping (Cell)
- Improved whole-chromosome phasing for disease and population genetic studies (Nature Methods)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
Their papers
- The Sorcerer II Global Ocean Sampling Expedition: Expanding the Universe of Protein Families (2007) — 858 citations
- The Diploid Genome Sequence of an Individual Human (2007) — 1,867 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- The Sequence of the Human Genome (2001) — 6,774 citations
- Inferring gene ontologies from pairwise similarity data (2014) — 87 citations
- HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies (2017) — 331 citations
- Extrachromosomal oncogene amplification drives tumor evolution and genetic heterogeneity (2017) — 727 citations
- De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly (2012) — 684 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations