Süleyman Cenk Sahinalp
Molecular Biology · 2009–2020
A researcher in the Science corpus: 7 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 107 citations into it; #13,614 of 17,773 by trust here, #4,409 by citations
Whom Süleyman Cenk Sahinalp trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Süleyman Cenk Sahinalp overall
Papers from Süleyman Cenk Sahinalp's perspective
Ordered by how strongly the researchers Süleyman Cenk Sahinalp trusts endorse each paper. Same corpus, a different order for every researcher.
- The complete genome of an individual by massively parallel DNA sequencing (Nature)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- Base-calling of automated sequencer traces using phred. II. Error probabilities.
- Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer (Nature)
- Landscape of somatic mutations in 560 breast cancer whole genome sequences (Nature)
- Whole-genome sequencing and variant discovery in C. elegans (Nature Methods)
- ARID1A mutations in endometriosis-associated ovarian carcinomas. (New England Journal of Medicine)
- The patterns and dynamics of genomic instability in metastatic pancreatic cancer (Nature)
Their papers
- Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (2009) — 789 citations
- mrsFast: a cache-oblivious algorithm for short-read mapping (2010) — 314 citations
- deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq Data (2011) — 562 citations
- Combinatorial Algorithms for Structural Variation Detection in High Throughput Sequenced Genomes (2009) — 331 citations
- The evolutionary history of 2,658 cancers (2017) — 937 citations
- PSORTb 3.0: improved protein subcellular localization prediction with refined localization subcategories and predictive capabilities for all prokaryotes (2010) — 2,426 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations