Ira M. Hall
Molecular Biology · 2002–2021
A researcher in the Science corpus: 11 papers; trusts 9 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 178 citations into it; #13,292 of 17,773 by trust here, #2,892 by citations
- Genetics — 131 citations into it; #5,318 of 6,854 by trust here, #1,101 by citations
- Plant Science — 47 citations into it
- Artificial Intelligence — 23 citations into it
Whom Ira M. Hall trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Ira M. Hall overall
Papers from Ira M. Hall's perspective
Ordered by how strongly the researchers Ira M. Hall 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
- A CENSUS OF HUMAN CANCER GENES (Nature Reviews. Cancer)
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (Nature Methods)
- Theoretical and practical advances in genome halving
- SomaticSniper: identification of somatic point mutations in whole genome sequencing data (Bioinform.)
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. (American Journal of Human Genetics)
- A whole-genome assembly of Drosophila. (Science)
- Mapping copy number variation by population scale genome sequencing (Nature)
Their papers
- Establishment and Maintenance of a Heterochromatin Domain (2002) — 902 citations
- LUMPY: a probabilistic framework for structural variant discovery (2012) — 1,443 citations
- The complete sequence of a human genome (2021) — 2,469 citations
- High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios (2021) — 932 citations
- Telomere-to-telomere assembly of a complete human X chromosome (2019) — 617 citations
- MOODS: fast search for position weight matrix matches in DNA sequences (2009) — 7,583 citations
- SVScore: an impact prediction tool for structural variation (2016) — 52 citations
- SAMBLASTER: fast duplicate marking and structural variant read extraction (2014) — 864 citations
- Haplotype-resolved diverse human genomes and integrated analysis of structural variation (2021) — 639 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations
- Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi (2002) — 2,172 citations