Chip Stewart
Molecular Biology · 2011–2020
A researcher in the Science corpus: 24 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 514 citations into it
- Genetics — 282 citations into it
- Artificial Intelligence — 20 citations into it
Whom Chip Stewart trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Chip Stewart's perspective
Ordered by how strongly the researchers Chip Stewart 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)
- Identification of common molecular subsequences.
- A CENSUS OF HUMAN CANCER GENES (Nature Reviews. Cancer)
- SOAP: short oligonucleotide alignment program (Bioinform.)
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- SomaticSniper: identification of somatic point mutations in whole genome sequencing data (Bioinform.)
- Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
- A Block-sorting Lossless Data Compression Algorithm
Their papers
- Mutational heterogeneity in cancer and the search for new cancer genes (2013) — 1,147 citations
- Evolution and impact of subclonal mutations in chronic lymphocytic leukemia (2013) — 1,402 citations
- The genetic landscape of high-risk neuroblastoma (2013) — 1,115 citations
- Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines (2018) — 746 citations
- Comprehensive molecular profiling of lung adenocarcinoma (2014) — 5,176 citations
- MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping (2013) — 295 citations
- Integrated Genomic Characterization of Papillary Thyroid Carcinoma (2014) — 2,692 citations
- Comprehensive Molecular Characterization of Urothelial Bladder Carcinoma (2014) — 2,001 citations
- Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors (2017) — 879 citations
- Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) — 508 citations
- Calling Somatic SNVs and Indels with Mutect2 (2019) — 613 citations
- Molecular Subtypes of Diffuse Large B-cell Lymphoma are Associated with Distinct Pathogenic Mechanisms and Outcomes (2018) — 1,686 citations
- SvABA: genome-wide detection of structural variants and indels by local assembly (2018) — 376 citations
- Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing (2018) — 609 citations
- Integrated Genomic Characterization of Pancreatic Ductal Adenocarcinoma (2017) — 1,688 citations
- Integrated genomic characterization of oesophageal carcinoma (2017) — 1,666 citations
- Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma (2016) — 908 citations
- Mutations driving CLL and their evolution in progression and relapse (2015) — 1,030 citations
- The molecular taxonomy of primary prostate cancer (2015) — 2,751 citations
- Prospective derivation of a Living Organoid Biobank of colorectal cancer patients (2015) — 2,171 citations