Search Results - "Stewart, Chip"
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RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues
Published in Science (American Association for the Advancement of Science) (07-06-2019)“…How somatic mutations accumulate in normal cells is poorly understood. A comprehensive analysis of RNA sequencing data from ~6700 samples across 29 normal…”
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2
SvABA: genome-wide detection of structural variants and indels by local assembly
Published in Genome research (01-04-2018)“…Structural variants (SVs), including small insertion and deletion variants (indels), are challenging to detect through standard alignment-based variant calling…”
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3
Somatic retrotransposition in human cancer revealed by whole-genome and exome sequencing
Published in Genome research (01-07-2014)“…Retrotransposons constitute a major source of genetic variation, and somatic retrotransposon insertions have been reported in cancer. Here, we applied…”
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4
MOSAIK: a hash-based algorithm for accurate next-generation sequencing short-read mapping
Published in PloS one (05-03-2014)“…MOSAIK is a stable, sensitive and open-source program for mapping second and third-generation sequencing reads to a reference genome. Uniquely among current…”
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5
Recurrent and functional regulatory mutations in breast cancer
Published in Nature (London) (06-07-2017)“…Genomic analysis of tumours has led to the identification of hundreds of cancer genes on the basis of the presence of mutations in protein-coding regions. By…”
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6
Clonal evolution in patients with chronic lymphocytic leukaemia developing resistance to BTK inhibition
Published in Nature communications (20-05-2016)“…Resistance to the Bruton’s tyrosine kinase (BTK) inhibitor ibrutinib has been attributed solely to mutations in BTK and related pathway molecules. Using…”
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7
Targetable genetic features of primary testicular and primary central nervous system lymphomas
Published in Blood (18-02-2016)“…Primary central nervous system lymphomas (PCNSLs) and primary testicular lymphomas (PTLs) are extranodal large B-cell lymphomas (LBCLs) with inferior responses…”
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8
Paired exome analysis of Barrett's esophagus and adenocarcinoma
Published in Nature genetics (01-09-2015)“…Adam Bass, Gad Getz, Scott Carter and colleagues report the whole-exome sequences of 25 pairs of esophageal adenocarcinoma and Barrett's esophagus. They…”
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9
Widespread Chromosomal Losses and Mitochondrial DNA Alterations as Genetic Drivers in Hürthle Cell Carcinoma
Published in Cancer cell (13-08-2018)“…Hürthle cell carcinoma of the thyroid (HCC) is a form of thyroid cancer recalcitrant to radioiodine therapy that exhibits an accumulation of mitochondria. We…”
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10
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation
Published in Nucleic acids research (01-04-2013)“…As researchers begin probing deep coverage sequencing data for increasingly rare mutations and subclonal events, the fidelity of next generation sequencing…”
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11
Evolution and Impact of Subclonal Mutations in Chronic Lymphocytic Leukemia
Published in Cell (14-02-2013)“…Clonal evolution is a key feature of cancer progression and relapse. We studied intratumoral heterogeneity in 149 chronic lymphocytic leukemia (CLL) cases by…”
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12
Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma
Published in Cell reports (Cambridge) (26-04-2016)“…Large-scale genomic characterization of tumors from prospective cohort studies may yield new insights into cancer pathogenesis. We performed whole-exome…”
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13
Genetic and Clonal Dissection of Murine Small Cell Lung Carcinoma Progression by Genome Sequencing
Published in Cell (13-03-2014)“…Small cell lung carcinoma (SCLC) is a highly lethal, smoking-associated cancer with few known targetable genetic alterations. Using genome sequencing, we…”
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14
The genomic landscape of pediatric Ewing sarcoma
Published in Cancer discovery (01-11-2014)“…Pediatric Ewing sarcoma is characterized by the expression of chimeric fusions of EWS and ETS family transcription factors, representing a paradigm for…”
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15
Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident
Published in Science (American Association for the Advancement of Science) (14-05-2021)“…Effects of radiation exposure from the Chernobyl nuclear accident remain a topic of interest. We investigated germline de novo mutations (DNMs) in children…”
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16
DeTiN: overcoming tumor-in-normal contamination
Published in Nature methods (01-07-2018)“…Comparison of sequencing data from a tumor sample with data from a matched germline control is a key step for accurate detection of somatic mutations…”
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Exome sequencing of lymphomas from three dog breeds reveals somatic mutation patterns reflecting genetic background
Published in Genome research (01-11-2015)“…Lymphoma is the most common hematological malignancy in developed countries. Outcome is strongly determined by molecular subtype, reflecting a need for new and…”
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18
Genomic signatures of past and present chromosomal instability in Barrett’s esophagus and early esophageal adenocarcinoma
Published in Nature communications (04-10-2023)“…The progression of precancerous lesions to malignancy is often accompanied by increasing complexity of chromosomal alterations but how these alterations arise…”
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Integrative and Comparative Genomic Analysis of Lung Squamous Cell Carcinomas in East Asian Patients
Published in Journal of clinical oncology (10-01-2014)“…Lung squamous cell carcinoma (SCC) is the second most prevalent type of lung cancer. Currently, no targeted therapeutics are approved for treatment of this…”
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20
Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma
Published in Cell reports (Cambridge) (18-10-2016)Get full text
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