SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
about
Multilevel genomics of colorectal cancers with microsatellite instability-clinical impact of JAK1 mutations and consensus molecular subtype 1Impact of mutations in Toll-like receptor pathway genes on esophageal carcinogenesis.Interpreting whole genome and exome sequencing data of individual gastric cancer samples.Mutation Processes in 293-Based Clones Overexpressing the DNA Cytosine Deaminase APOBEC3B.Exome sequencing of osteosarcoma reveals mutation signatures reminiscent of BRCA deficiencyAncestral-derived effects on the mutational landscape of laryngeal cancer.Patient-specific factors influence somatic variation patterns in von Hippel-Lindau disease renal tumours.Merkel Cell Polyomavirus Exhibits Dominant Control of the Tumor Genome and Transcriptome in Virus-Associated Merkel Cell Carcinoma.Deep targeted sequencing in pediatric acute lymphoblastic leukemia unveils distinct mutational patterns between genetic subtypes and novel relapse-associated genes.Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance.Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline CHEK2:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinoma.Exploring background mutational processes to decipher cancer genetic heterogeneity.Understanding mutagenesis through delineation of mutational signatures in human cancer.Genomic landscape of colorectal cancer in Japan: clinical implications of comprehensive genomic sequencing for precision medicine.Mutational Signatures in Breast Cancer: The Problem at the DNA LevelBRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers.Selective analysis of cancer-cell intrinsic transcriptional traits defines novel clinically relevant subtypes of colorectal cancer.Clonal selection and double-hit events involving tumor suppressor genes underlie relapse in myeloma.Genomic profiles of a hepatoblastoma from a patient with Beckwith-Wiedemann syndrome with uniparental disomy on chromosome 11p15 and germline mutation of APC and PALB2.Comparative genomics reveals that loss of lunatic fringe (LFNG) promotes melanoma metastasis.mSignatureDB: a database for deciphering mutational signatures in human cancers.Mutational patterns in chemotherapy resistant muscle-invasive bladder cancer.Whole exome sequencing identified sixty-five coding mutations in four neuroblastoma tumors.Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer.The ubiquitous 'cancer mutational signature' 5 occurs specifically in cancers with deleted FHIT alleles.Genome-wide genetic and epigenetic analyses of pancreatic acinar cell carcinomas reveal aberrations in genome stability.Aristolochic acids and their derivatives are widely implicated in liver cancers in Taiwan and throughout Asia.Nuclear topology modulates the mutational landscapes of cancer genomes.Mutational signatures and chromosome alteration profiles of squamous cell carcinomas of the vulva.NSAID use and somatic exomic mutations in Barrett's esophagus.A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers.Whole exome sequencing identifies mTOR and KEAP1 as potential targets for radiosensitization of HNSCC cells refractory to EGFR and β1 integrin inhibition.Characterization of BK Polyomaviruses from Kidney Transplant Recipients Suggests a Role for APOBEC3 in Driving In-Host Virus Evolution.Genomic features of renal cell carcinoma with venous tumor thrombus.The effects of mutational processes and selection on driver mutations across cancer types.MutationalPatterns: comprehensive genome-wide analysis of mutational processes.Somatic Mitochondrial DNA Mutations in Diffuse Large B-Cell Lymphoma.Validating the concept of mutational signatures with isogenic cell models.Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants.Evolutionary history of metastatic breast cancer reveals minimal seeding from axillary lymph nodes.
P2860
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P2860
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
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2015年學術文章
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2015年學術文章
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name
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@en
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@nl
type
label
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@en
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@nl
prefLabel
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@en
SomaticSignatures: inferring mutational signatures from single-nucleotide variants.
@nl
P2860
P356
P1433
P1476
SomaticSignatures: inferring mutational signatures from single-nucleotide variants
@en
P2093
Bernd Fischer
Michael Lawrence
P2860
P304
P356
10.1093/BIOINFORMATICS/BTV408
P407
P577
2015-07-10T00:00:00Z