Hello Gene Pattern team,
I am seeking help with a reproducible Floating point exception when running GISTIC 2.0.23 to identify significant copy-number alteration (CNA) peaks from a large WES cohort.
Data type: Whole-exome sequencing (WES)
Cohort size: >600 tumor samples
CNA segmentation was performed prior to GISTIC, and all samples are included in a single seg file.
GISTIC version: 2.0.23
Reference genome: hg38
Command used:./gistic2 -b /WorkSpace/liukun/Test/Test1 -seg /WorkSpace/liukun/Test/Test1/GISTIC.input.txt -refgene /XSoftware/GISTIC2.0/refgenefiles/hg38.UCSC.add_miR.160920.refgene.mat -genegistic 1 -gcm extreme -rx 0 -brlen 0.5 -broad 1 -conf 0.95 -armpeel 1 -smallmem 0 -savegene 1 -qvt 0.1
GISTIC terminates with a Floating point exception during execution.
The detailed runtime output and stack trace are provided in output.log (https://drive.google.com/file/d/1E9e9u_EYuuNA3NnzkHKDXOi75bMrzICO/view?usp=sharing).
Finding peaks on chromosome 21
------------------------------------------------------------------------
Floating point exception detected at Wed Feb 4 09:32:45 2026
------------------------------------------------------------------------
Configuration:
Crash Decoding : Disabled
Current Visual : None
Default Encoding : UTF-8
GNU C Library : 2.35 stable
MATLAB Architecture: glnxa64
MATLAB Root : /WorkSpace/liukun/Software/GISTIC2.0/MATLAB_Compiler_Runtime/v83
MATLAB Version : 8.3.0.532 (R2014a)
Operating System : Linux 5.15.0-164-generic #174-Ubuntu SMP Fri Nov 14 20:25:16 UTC 2025 x86_64
Processor ID : x86 Family 6 Model 106 Stepping 6, GenuineIntel
Virtual Machine : Java 1.7.0_11-b21 with Oracle Corporation Java HotSpot(TM) 64-Bit Server VM mixed mode
Window System : No active display
Fault Count: 1
Abnormal termination:
Floating point exception
The crash consistently occurs during focal peak analysis (e.g., while processing individual chromosomes), suggesting a numerical issue rather than a file I/O or environment problem.
The seg file (GISTIC.input.txt, https://drive.google.com/file/d/1mF8OEQwQ7iTuHId75nbtRq3MGO7q2odT/view?usp=sharing) used for this run is attached.
All segment mean values are finite (no Inf, -Inf, or NaN).
Chromosomes are encoded numerically (1–22).
Very short segments and obvious outliers have been filtered.
Given the large cohort size (>600 samples), I would like to ask:
In this context, I would appreciate guidance on how to adjust the GISTIC parameter settings to ensure that the analysis can run successfully. Specifically, are there recommended parameter choices for large WES-based cohorts to avoid numerical instability during focal peak calling?
Any guidance on recommended parameter adjustments or known bugs would be greatly appreciated.
For whole-exome sequencing (WES) data, the definition of Num Markers in the seg file is not entirely clear.
Currently, following the implementation in
https://github.com/sbamin/canine_gistic2/blob/master/make_segments.R,
I set the number of markers as:
I would like to ask whether this setting is reasonable for WES-based CNA segmentation.
Specifically, for WES data, how should Num Markers in the GISTIC seg file be defined in a principled way?
Thank you very much for your time and for maintaining GISTIC.
I would be happy to provide additional information or a minimal reproducible example if needed.
Best regards,
Kun Liu
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