Integrated analysis of gene expression and copy number alterations.

Slides:



Advertisements
Similar presentations
What do we already know ? The rice disease resistance gene Pi-ta Genetically mapped to chromosome 12 Rybka et al. (1997). It has also been sequenced Bryan.
Advertisements

Supplementary Figure 1 List of top 50 most abundantly expressed lncRNAs and mRNAs in HP and PFC from RNAseq. Expression abundance of lncRNAs and mRNAs.
Homozygous deletions within chromosome 9q23.
The cBio Cancer Genomics Portal.
Fig. 8. Recurrent copy number amplification of BRD4 gene was observed across common cancers. Recurrent copy number amplification of BRD4 gene was observed.
BCR–ABL1 B-ALLs feature DNA methylation and expression signatures centered aroundIL2RA(CD25). BCR–ABL1 B-ALLs feature DNA methylation and expression signatures.
Volume 10, Issue 6, Pages (December 2006)
Genomic alterations in breast cancer cell line MDA-MB-231.
by Gregory H. Underhill, David George, Eric G. Bremer, and Geoffrey S
Copy-number alterations in an archival breast cancer sample.
FGFR and PRKA gene rearrangements in CCAs
Genomic rearrangements of E
Identification of TLOC1 and SKIL as tumor driver genes in 3q26.
CHK1 downregulation upon ERG overexpression.
Patterns of Somatically Acquired Amplifications and Deletions in Apparently Normal Tissues of Ovarian Cancer Patients  Leila Aghili, Jasmine Foo, James.
Diverse abnormalities manifest in RNA
Epigenetic regulation of miR-193b in liposarcomagenesis.
Whole-exome sequencing identifies NF1 mutations in tumors of melanoma patients exhibiting resistance to vemurafenib. Whole-exome sequencing identifies.
Volume 24, Issue 4, Pages (July 2018)
Volume 23, Issue 1, Pages 9-22 (January 2013)
PD-1 expression on HCC-infiltrating B cells and its clinical significance. PD-1 expression on HCC-infiltrating B cells and its clinical significance. A–H,
Cluster analysis and pathway-based characterization of differentially expressed genes and proteins from integrated proteomics. Cluster analysis and pathway-based.
Histology and genomic copy number alterations in TRAMP tumors.
Distribution of informative SNPs with LOH (black bars) on each chromosome (rows, oriented p-arm at the bottom and q-arm at the top of each chromosome)
Bar plot representation of the transcriptomic changes in Δsaci_ptp and Δsaci_pp2a. Bar plot representation of the transcriptomic changes in Δsaci_ptp and.
Validation of RNA transcription profile differential expression using real-time quantitative PCR. Relative gene expression in cases compared with controls.
Phylogenetic tree of 38 Pseudomonas type strains, based on the V3-V5 region sequence of the 16S rRNA gene (V3 primer, positions 442 to 492; and V5 primer,
Elisha D. O. Roberson, Ying Liu, Caitriona Ryan, Cailin E
Comparison of proteomics and RNA‐Seq data.
Volume 10, Issue 6, Pages (December 2006)
Identification and characterization of a novel KRAS rearrangement in metastatic prostate cancer. Identification and characterization of a novel KRAS rearrangement.
LDL2 functions downstream of ibm1‐induced ectopic H3K9me2 and non‐CG methylation LDL2 functions downstream of ibm1‐induced ectopic H3K9me2 and non‐CG methylation.
A multitiered approach to characterize transcriptome structure.
Identification of the CD74–NRG1 fusion gene.
Differential binding of H3K36me3 in G34-mutant KNS42 cells drives pediatric GBM expression signatures. Differential binding of H3K36me3 in G34-mutant KNS42.
Patterns and regulation of age‐related splicing changes.
LDL2 functions downstream of ibm1‐induced ectopic H3K9me2 and non‐CG methylation LDL2 functions downstream of ibm1‐induced ectopic H3K9me2 and non‐CG methylation.
Patterns of Somatically Acquired Amplifications and Deletions in Apparently Normal Tissues of Ovarian Cancer Patients  Leila Aghili, Jasmine Foo, James.
CD4-TEMRA cells show marked clonal expansion.
RNAseq–Volcano plots, qPCR validation, and GO enrichment analysis.
Analysis of renal transcriptome responses identifies LX-regulated transcriptional networks. Analysis of renal transcriptome responses identifies LX-regulated.
Structure of Wt1 genomic regions in human and zebrafish.
Volume 41, Issue 2, Pages (January 2011)
Diagnostic plots of the TGI PKPD model fitted to the A677 TGI data.
Methylation status of IGFBPL1 in human breast cancer.
Influence of RdDM on DCL4 Transcript Isoform Expression.
EZH2 overexpression establishes a unique and conserved super-enhancer–associated transcriptional landscape. EZH2 overexpression establishes a unique and.
Integrated mRNA and microRNA expression and DNA methylation clusters.
Heat map of genes for which CR significantly altered expression versus AL. Cluster analysis of genes significantly changed by the CR intervention compared.
Immune activity and neopeptide load correlate across tumor types.
Sample-wise outlier kinases in ERBB2-positive breast cancer cell lines
Pancreatic cancer cell lines are sensitive to knockdown of outlier kinases. Pancreatic cancer cell lines are sensitive to knockdown of outlier kinases.
Transcriptional and genomic targets of EN1 in TNBC cells.
Specific DNA methylation and expression signatures associated with binding of E2A–PBX1 fusion protein. Specific DNA methylation and expression signatures.
Initial testing and characterization of cAMPr in ES cells.
Clustering analysis of DTC-associated genes.
Landscape of genomic alterations identified by WES in biopsies of patients with advanced PDAC. Co-mutation plot displaying integrated genomic data for.
Germline variants influencing primary tumor type.
A, heatmap of copy number alterations determined by array CGH for a panel of 79 frozen NSCLC samples. A, heatmap of copy number alterations determined.
Distinct subtypes of CAFs are detected in human PDAC
Single-cell analysis uncovers ductal cell subpopulations in human PDAC
EZH2-driven lung cancer as a molecularly distinct entity.
Gene expression heatmap of non–T-cell-inflamed, intermediate, and T-cell–inflamed testicular germ cell tumors from TCGA. Genes are on the row, and samples.
High genomic fidelity of SCLC PDX models derived from both CTCs and biopsies. High genomic fidelity of SCLC PDX models derived from both CTCs and biopsies.
Driver pathways and key genes in OSCC
CASP8 mutations are associated with fewer CNAs and RAS family mutations. CASP8 mutations are associated with fewer CNAs and RAS family mutations. A, number.
Mutant TERT promoter displays active histone marks and distinct long-range interactions: A, cell lines that were used in the study with their origin and.
REV-ERBα deficiency alters the epigenetic landscape and differentially affects clock gene expression in ILC3 subsets. REV-ERBα deficiency alters the epigenetic.
Relative abundance and expression of the 10 most abundant MAGs in the bioreactor at day 96. Relative abundance and expression of the 10 most abundant MAGs.
Comparison of shRNA scoring approaches.
Presentation transcript:

Integrated analysis of gene expression and copy number alterations. Integrated analysis of gene expression and copy number alterations. A, copy number (CN) and outlier gene expression plot. Frequency indicates how often a gene with the indicated relative copy number shows low, normal, or high transcript expression. Frequencies were calculated from all genes and all samples with the indicated relative copy number. High or low expression identifies samples outside of the 95% confidence interval for expression as described in B. B, gene expression versus copy number for CCND1. Each dot represents one sample. Black horizontal bars designate gene expression mean. Red bars indicate the 95% confidence interval of gene expression for samples with relative CN = 0. C, modified Integrative Genomics Viewer plot for the region around CCND1. Chromosome location is shown at the top. Each row is a sample and the relative copy number is indicated by color. Black boxes around a gene indicate it as an outlier with respect to expression. ID, identifier sequence. Curtis R. Pickering et al. Cancer Discovery 2013;3:770-781 ©2013 by American Association for Cancer Research