Christopher T. Saunders
Genetics · 2002–2018
A researcher in the Science corpus: 4 papers; trusts 4 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 20 citations into it; #1,759 of 6,854 by trust here, #2,249 by citations
- Molecular Biology — 19 citations into it; #5,663 of 17,773 by trust here, #9,851 by citations
- Computational Biology & Bioinformatics — 6 citations into it
Whom Christopher T. Saunders trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Amos Bairoch
- Pauline Crystal Ng
- W. Kabsch
- Burkhard Rost
- Steven Henikoff
- Christopher Sander
- Shamil R. Sunyaev
- Rolf Apweiler
- John Moult
- V. Ramensky
Who trusts Christopher T. Saunders overall
- Pauline Crystal Ng
- Yana Bromberg
- Steven Henikoff
- Vanessa E. Gray
- Biao Li
- Burkhard Rost
- Ronald J. Hause
- Jeffrey R. Brender
- Vidhya Gomathi Krishnan
- J. Thusberg
Papers from Christopher T. Saunders's perspective
Ordered by how strongly the researchers Christopher T. Saunders trusts endorse each paper. Same corpus, a different order for every researcher.
- The SWISS-PROT protein sequence data bank and its supplement TrEMBL
- Prediction of deleterious human alleles.
- Predicting deleterious amino acid substitutions.
- SNPs, protein structure, and disease
- Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation.
- Systematic mutation of bacteriophage T4 lysozyme.
- Selection of representative protein data sets
- Conservation and prediction of solvent accessibility in protein families
- Dictionary of protein secondary structure: Pattern recognition of hydrogen‐bonded and geometrical features
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
Their papers
- Evaluation of structural and evolutionary contributions to deleterious mutation prediction. (2002) — 213 citations
- Isaac: ultra-fast whole-genome secondary analysis on Illumina sequencing platforms (2013) — 336 citations
- Strelka2: fast and accurate calling of germline and somatic variants (2018) — 1,345 citations
- Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications (2016) — 1,944 citations