Li Ding
Molecular Biology · Nature · 2007–2020
A researcher in the Science corpus: 59 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 904 citations into it
- Computational Biology & Bioinformatics — 44 citations into it
- Spectroscopy — 42 citations into it
Whom Li Ding trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Li Ding overall
- Charles Swanton
- Hans Clevers
- Daniel C. Koboldt
- Katharina Jahn
- Jason A. Reuter
- Michael R. Stratton
- Heng Li
Papers from Li Ding's perspective
Ordered by how strongly the researchers Li Ding trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- KEGG: Kyoto Encyclopedia of Genes and Genomes (Nucleic Acids Res.)
- ARID1A mutations in endometriosis-associated ovarian carcinomas. (New England Journal of Medicine)
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (Nature Methods)
- Tumour evolution inferred by single-cell sequencing (Nature)
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (Nature Genetics)
- Supervised risk predictor of breast cancer based on intrinsic subtypes.
- GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers (Genome Biology)
- BCR–ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros (Nature)
Their papers
- Identification of a CpG island methylator phenotype that defines a distinct subgroup of glioma. (2010) — 2,267 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- BreakDancer: An algorithm for high resolution mapping of genomic structural variation (2009) — 1,513 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- An integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR and NF1 (2010) — 7,152 citations
- Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome (2009) — 2,302 citations
- Mutational landscape and significance across 12 major cancer types (2013) — 4,262 citations
- VarScan: variant detection in massively parallel sequencing of individual and pooled samples (2009) — 1,343 citations
- Somatic mutations affect key pathways in lung adenocarcinoma (2008) — 2,751 citations
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012) — 4,654 citations
- Comprehensive molecular portraits of human breast tumors (2012) — 7,518 citations
- Comprehensive Molecular Characterization of Human Colon and Rectal Cancer (2012) — 7,754 citations
- Characterizing the cancer genome in lung adenocarcinoma (2007) — 1,146 citations
- RECURRENT MUTATIONS IN THE U2AF1 SPLICING FACTOR IN MYELODYSPLASTIC SYNDROMES (2011) — 594 citations
- Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients (2018) — 792 citations
- The origin and evolution of mutations in Acute Myeloid Leukemia (2012) — 1,580 citations
- Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines (2018) — 746 citations
- MuSiC: Identifying mutational significance in cancer genomes (2012) — 667 citations
- DGIdb - Mining the druggable genome (2013) — 505 citations
- Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) — 7,050 citations