Allegra Petti
Genetics · 2015–2016
A researcher in the Science corpus: 4 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 21 citations into it
Whom Allegra Petti trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Allegra Petti's perspective
Ordered by how strongly the researchers Allegra Petti trusts endorse each paper. Same corpus, a different order for every researcher.
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- Integrative Genomics Viewer (Nature Biotechnology)
- Prediction of MHC class I binding peptides using profile motifs. (Human Immunology)
- NetMHCpan, a Method for Quantitative Predictions of Peptide Binding to Any HLA-A and -B Locus Protein of Known Sequence
- The immune epitope database (IEDB) 3.0 (Nucleic Acids Res.)
- SomaticSniper: identification of somatic point mutations in whole genome sequencing data (Bioinform.)
- NetMHCpan, a method for MHC class I binding prediction beyond humans
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Strelka: accurate somatic small-variant calling from sequenced tumor-normal sample pairs (Bioinform.)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
Their papers
- RNA splicing is a primary link between genetic variation and disease (2016) — 634 citations
- A dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells (2015) — 1,091 citations
- pVAC-Seq: A genome-guided in silico approach to identifying tumor neoantigens (2016) — 392 citations
- TP53 and Decitabine in Acute Myeloid Leukemia and Myelodysplastic Syndromes (2016) — 731 citations