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Journal: STAR Protocols
Article Title: Identifying tumorigenic non-coding mutations through altered cis -regulation
doi: 10.1016/j.xpro.2021.100934
Figure Lengend Snippet: Screenshot of how to add the Driver_ASE scripts into the MATLAB global path
Article Snippet: The pipeline uses different perl scripts to download SNP array, RNA-Seq and WGS BAMs, and then calculate gene-level ASE and call somatic mutations; these results are then converted to associate somatic mutations in different regulatory elements and
Techniques:
Journal: STAR Protocols
Article Title: Identifying tumorigenic non-coding mutations through altered cis -regulation
doi: 10.1016/j.xpro.2021.100934
Figure Lengend Snippet: Sample MATLAB commands to run ASE-Mut association on BRCA data
Article Snippet: The pipeline uses different perl scripts to download SNP array, RNA-Seq and WGS BAMs, and then calculate gene-level ASE and call somatic mutations; these results are then converted to associate somatic mutations in different regulatory elements and
Techniques:
Journal: STAR Protocols
Article Title: Identifying tumorigenic non-coding mutations through altered cis -regulation
doi: 10.1016/j.xpro.2021.100934
Figure Lengend Snippet: Evaluation of ASE-Mutation associations using the MATLAB function ‘ M1_Import_ASE_and_Mutation_data.m ’ Typing ‘Top_assoc’ in MATLAB terminal shows the top associations (false discovery rate [FDR]<=0.2 and raw association p value [p]<=0.05) across 18 different regulatory or genomic features after running the scripts in this vignette with default settings. All association results are also included in the MATLAB structure ‘All_Assoc’.
Article Snippet: The pipeline uses different perl scripts to download SNP array, RNA-Seq and WGS BAMs, and then calculate gene-level ASE and call somatic mutations; these results are then converted to associate somatic mutations in different regulatory elements and
Techniques: Mutagenesis
Journal: STAR Protocols
Article Title: Identifying tumorigenic non-coding mutations through altered cis -regulation
doi: 10.1016/j.xpro.2021.100934
Figure Lengend Snippet: The directory tree of the final ASE-Mutation results (A) The ASE-Mutation associations are saved in the ‘BRCA’ directory that includes 3 subdirectories: ‘Driver_Beds’, ‘hits’, and ‘mut_ase_auto’. After running the pipeline the ‘Driver_beds’ directory will contain one text file of all associations FDR<0.2 (driver_top_fdr0.2), and a bed file for each association between a mutated cis-regulatory element and gene-level ASE. For example, the upper box shows an association between RALGPS1 and mutations within 10kb of its TSS and gene body that is found using the demo data of 46 BRCA samples. The bed files of putative driver mutations can be visualized with the UCSC or alternate genome browsers (hg19). The directory ‘hits’ will contain all ASE-Mut association results as shown in the lower panel. (B) The raw association p-values (assoc_P_all.tab), FDR values (fdr_all.tab), mutation enrichment p-values for each feature with each gene (fm_all.tab), and information for samples harboring these regulatory mutations (mut_all.tab) are output into the ‘hits’ directory. The ‘mut_ase_auto’ directory contains the ‘mutation x regulatory-feature’ MATLAB matrix.
Article Snippet: The pipeline uses different perl scripts to download SNP array, RNA-Seq and WGS BAMs, and then calculate gene-level ASE and call somatic mutations; these results are then converted to associate somatic mutations in different regulatory elements and
Techniques: Mutagenesis