CHASM 1.0.5 (Cancer-Specific High-throughput Annotation of Somatic Mutations)
Thymoma (Primary solid tumor)
28 January 2016  |  analyses__2016_01_28
Maintainer Information
Citation Information
Maintained by Spring Yingchun Liu (Broad Institute)
Cite as Broad Institute TCGA Genome Data Analysis Center (2016): CHASM 1.0.5 (Cancer-Specific High-throughput Annotation of Somatic Mutations). Broad Institute of MIT and Harvard. doi:10.7908/C1NV9HSH
Overview
Introduction

CHASM is a method that predicts the functional significance of somatic missense mutations observed in the genomes of cancer cells, allowing mutations to be prioritized in subsequent functional studies, based on the probability that they give the cells a selective survival advantage [2].

Summary

There are 1379 mutations identified by MuTect and 99 mutations with significant functional impact at BHFDR <= 0.25.

Results
Top Mutations

Table 1.  Get Full Table Top mutations with significant funcational impact.
MutationID: mutation seen in sample.
Mutation: mutation seen in gene and AA variant.
CHASM: CHASM score.
BHFDR: Benjamini-Hochberg False Discovery Rate.

MutationID Mutation CHASM PValue BHFDR
TCGA-ZB-A966-01A-11D-A428-09 NM_021913.3_R671L 0.18 0 0.05
TCGA-X7-A8D6-01A-11D-A423-09 NM_001145306.1_A63T 0.17 0 0.05
TCGA-ZB-A966-01A-11D-A428-09 NM_001274.4_G72V 0.2 0.001 0.05
TCGA-XU-A92Z-01A-11D-A423-09 NM_014280.2_A125S 0.2 0.001 0.05
TCGA-5U-AB0E-01A-11D-A423-09 NM_182562.2_Y56H 0.2 0.001 0.05
Methods & Data
About CHASM

CHASM uses a machine learning method called Random Forest that learns to distinguish between driver and passenger somatic missense mutations, based on a training set of labeled positive (driver) and negative (passenger) examples. The positive class of driver mutations was curated from the COSMIC database and the negative class is composed of synthetic passenger mutations. CHASM annotates mutations with amino acid substitution properties, alignment-based estimates of conservation at the mutated position. The user provides a list of mutations for prediction as well as a table describing the passenger mutation spectrum for the tumor type in which the mutations were observed [1].

Download Results

In addition to the links below, the full results of the analysis summarized in this report can also be downloaded programmatically using firehose_get, or interactively from either the Broad GDAC website or TCGA Data Coordination Center Portal.