Gregory G. Faust
Molecular Biology · 2014
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 12 citations into it
Whom Gregory G. Faust trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Gregory G. Faust's perspective
Ordered by how strongly the researchers Gregory G. Faust 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)
- 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
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
- CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. (Genome Research)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- DGIdb - Mining the druggable genome (Nature Methods)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (Genome Research)
- The landscape of kinase fusions in cancer (Nature Communications)
Their papers
- SAMBLASTER: fast duplicate marking and structural variant read extraction (2014) — 864 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations