tLOH
tLOH assesses evidence for loss of heterozygosity (LOH) in pre-processed spatial transcriptomics data by calculating Bayes factors at likely heterozygous single-nucleotide polymorphism (SNP) positions.
Key Features:
- Bayes factor calculation: Bayes factors are calculated at each SNP to determine likelihood of potential loss of heterozygosity event.
- Allele fraction visualization: A plotting function visualizes allele fraction per chromosome.
- Aggregated Bayes factor visualization: A plotting function visualizes aggregated Bayes factor per chromosome.
- VCF input support: The tool requires spatial transcriptomics cluster and allele count information at likely heterozygous SNP positions in VCF format with required fields allele depth (AD) with counts for reference/alternative alleles and read depth (DP).
- 10X Genomics Visium compatibility: Data generated with the 10X Genomics Visium Spatial Gene Expression platform must be pre-processed to obtain an individual sample VCF with columns for each cluster.
Scientific Applications:
- Loss of heterozygosity detection: tLOH assesses evidence for loss of heterozygosity (LOH) in spatial transcriptomics data at the cluster level.
- Spatial transcriptomics analysis: The tool enables investigation of LOH events in spatially resolved transcriptomics data from the 10X Genomics Visium Spatial Gene Expression platform.
Methodology:
Bayes factors are calculated at each SNP to determine likelihood of potential loss of heterozygosity event.
Collections
Details
- License:
- MIT
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Mac, Windows
- Programming Languages:
- R
- Added:
- 10/2/2026
- Last Updated:
- 10/2/2026
Operations
Documentation
User manual
https://bioconductor.org/packages/tLOHDownloads
- Source codehttps://github.com/USCDTG/tLOH