Shilpa Garg
Genetics · 2016–2022
A researcher in the Science corpus: 4 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 57 citations into it
Whom Shilpa Garg trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Shilpa Garg's perspective
Ordered by how strongly the researchers Shilpa Garg 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
- Merlin—rapid analysis of dense genetic maps using sparse gene flow trees (Nature Genetics)
- Haplotype phasing: Existing methods and new developments (Nature reviews genetics)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- Diversity of Human Copy Number Variation and Multicopy Genes (Science)
- A linear complexity phasing method for thousands of genomes (Nature Methods)
- Resolving the complexity of the human genome using single-molecule sequencing (Nature)
- The mutational constraint spectrum quantified from variation in 141,456 humans
- A universal SNP and small-indel variant caller using deep neural networks
- Limitations of next-generation genome sequence assembly (Nature Methods)
Their papers
- Variation graph toolkit improves read mapping by representing genetic variation in the reference (2018) — 681 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- A draft human pangenome reference (2022) — 882 citations
- WhatsHap: fast and accurate read-based phasing (2016) — 406 citations