Colby Chiang
Molecular Biology · 2012–2017
A researcher in the Science corpus: 4 papers; trusts 2 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 69 citations into it; #11,902 of 17,773 by trust here, #4,377 by citations
- Artificial Intelligence — 8 citations into it
Whom Colby Chiang trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Alexej Abyzov
- Genome analysis
- Tobias Rausch
- Ryan M. Layer
- Umadevi Paila
- Nicolas Stransky
- Brad A. Chapman
- Daniel C. Koboldt
- Alexander E. Urban
Who trusts Colby Chiang overall
Papers from Colby Chiang's perspective
Ordered by how strongly the researchers Colby Chiang 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
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (Nature Methods)
- A CENSUS OF HUMAN CANCER GENES (Nature Reviews. Cancer)
- Mapping copy number variation by population scale genome sequencing (Nature)
- SomaticSniper: identification of somatic point mutations in whole genome sequencing data (Bioinform.)
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. (Genome Research)
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
- CREST maps somatic structural variation in cancer genomes with base-pair resolution (Nature Methods)
- Theoretical and practical advances in genome halving
Their papers
- LUMPY: a probabilistic framework for structural variant discovery (2012) — 1,443 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations