Nicolas Stransky
Molecular Biology · 2004–2019
A researcher in the Science corpus: 17 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 272 citations into it
- Artificial Intelligence — 9 citations into it
Whom Nicolas Stransky trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Nicolas Stransky overall
Papers from Nicolas Stransky's perspective
Ordered by how strongly the researchers Nicolas Stransky trusts endorse each paper. Same corpus, a different order for every researcher.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- STAR: ultrafast universal RNA-seq aligner (Bioinform.)
- Assembly of microarrays for genome-wide measurement of DNA copy number (Nature Genetics)
- Near-optimal probabilistic RNA-seq quantification (Nature Biotechnology)
- ABySS: a parallel assembler for short read sequence data. (Genome Research)
- Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling (Nature)
- MapSplice: Accurate mapping of RNA-seq reads for splice junction discovery (Nucleic Acids Research)
- Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. (Cancer Cell)
- The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (Nature)
Their papers
- The Cancer Cell Line Encyclopedia enables predictive modeling of anticancer drug sensitivity (2012) — 7,455 citations
- Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer (2012) — 1,524 citations
- The Mutational Landscape of Head and Neck Squamous Cell Carcinoma (2011) — 2,541 citations
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
- Melanoma genome sequencing reveals frequent PREX2 mutations (2012) — 752 citations
- Functional genomics reveals serine synthesis is essential in PHGDH-amplified breast cancer (2011) — 940 citations
- A Landscape of Driver Mutations in Melanoma (2012) — 2,528 citations
- An interactive resource to identify cancer genetic and lineage dependencies targeted by small molecules (2013) — 761 citations
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) — 7,050 citations
- Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing (2012) — 1,002 citations
- Sequence analysis of mutations and translocations across breast cancer subtypes (2012) — 1,207 citations
- Analysis of array CGH data: from signal ratio to gain and loss of DNA regions (2004) — 573 citations
- Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma (2017) — 2,216 citations
- COT/MAP3K8 drives resistance to RAF inhibition through MAP kinase pathway reactivation (2010) — 731 citations
- Next-generation characterization of the Cancer Cell Line Encyclopedia (2019) — 2,830 citations
- Accuracy assessment of fusion transcript detection via read-mapping and de novo fusion transcript assembly-based methods (2019) — 532 citations
- The landscape of kinase fusions in cancer (2014) — 890 citations