Whole-exome sequencing identifies multiple loss-of-function mutations of NF-κB pathway regulators in nasopharyngeal carcinoma | PNAS
IJMS | Free Full-Text | Whole Exome Sequencing Identifies a Novel Hedgehog-Interacting Protein G516R Mutation in Locally Advanced Papillary Thyroid Cancer
Genome / Exome sequencing
Cancer Exome Sequencing | Insight into coding mutations
Exome sequencing identifies somatic mutations in novel driver genes in non-small cell lung cancer - Figure f1 | Aging
JCI - Integrated RNA and DNA sequencing reveals early drivers of metastatic breast cancer
Identification of Variants in Primary and Recurrent Glioblastoma Using a Cancer-Specific Gene Panel and Whole Exome Sequencing | PLOS ONE
Comparison of whole-exome sequencing of cfDNA to whole-exome sequencing... | Download Scientific Diagram
Whole exome sequencing predicts whether patie | EurekAlert!
Computational analysis of cancer genome sequencing data | Nature Reviews Genetics
Cancers | Free Full-Text | Comprehensive Outline of Whole Exome Sequencing Data Analysis Tools Available in Clinical Oncology
Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome | Nature Communications
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples | Nature Communications
New Genomic Analysis of Immune Cell Infiltration in Colorectal Cancer
Optimizing Cancer Genome Sequencing and Analysis: Cell Systems
IJMS | Free Full-Text | A Pilot Study for the Feasibility of Exome- Sequencing in Circulating Tumor Cells Versus Single Metastatic Biopsies in Breast Cancer
Implementation and use of whole exome sequencing for metastatic solid cancer - eBioMedicine
Cancers | Free Full-Text | Comprehensive Outline of Whole Exome Sequencing Data Analysis Tools Available in Clinical Oncology
Multi-region exome sequencing reveals the intratumoral heterogeneity of surgically resected small cell lung cancer | Nature Communications
Whole-exome sequencing analysis of NSCLC reveals the pathogenic missense variants from cancer-associated genes - ScienceDirect
Comprehensive profiling of 1015 patients' exomes reveals genomic-clinical associations in colorectal cancer | Nature Communications
Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux - BioCode
Whole Exome Sequencing | Caris Life Sciences
Cancer genome sequencing - Wikipedia
