Related Experiment Video
Updated: Oct 5, 2026

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER
Published on: June 23, 2012
ChoCallate: a computational pipeline for consensus germline variant calling in genomic sequencing data
Aleksey Ermolaev1, Mikhail Divashuk1
1All-Russian Research Institute of Agricultural Biotechnology, Moscow, Russia.
Abstract:
Accurate germline variant calling in non-model and polyploid organisms remains challenging due to sequencing errors, genomic complexity, and caller-specific biases. Existing ensemble methods of variant calling are constrained by species-specific training, limited portability, or an inability to process multiple samples concurrently. To address these limitations we developed ChoCallate, a Nextflow-based pipeline for consensus germline variant calling. The pipeline integrates three species-independent callers, bcftools, FreeBayes, and Genome Analysis Toolkit (GATK) HaplotypeCaller, within a flexible voting mechanism. A distinctive feature of ChoCallate is its incorporation of coverage-aware consensus generation via Browser Extensible Data (BED) file, enabling reliable variant identification even in reduced-representation sequencing data such as Restriction site Associated DNA sequencing (RAD-seq) or RNA-seq. In a simulated dataset containing 10,000 single-nucleotide polymorphisms (SNPs) and 1,000 InDels of Arabidopsis thaliana across coverage depths ranging from 3× to 50×, the two-vote consensus strategy provided a favourable precision-recall balance, particularly at lower coverage (3×-10×), where SNP precision was enhanced without substantial loss of sensitivity. False-negative variants were found to concentrate in centromeric and nucleolus organizer regions (NORs) across all strategies, indicating that repetitive genomic structure, rather than consensus logic, constitutes the primary limitation. In a case study of 200 bread wheat (Triticum aestivum) samples, ChoCallate identified 11,178 high-confidence variants, and a genome-wide association study (GWAS) for awnedness successfully recovered the known B1/ALI-1 locus on chromosome 5A, replicating prior findings with reduced genomic inflation (λ (gc) = 1.06) by decreasing the number of false-positive variants through a consensus-based approach. ChoCallate is portable, species-agnostic, and freely available.
More Related Videos
11:02Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
Published on: October 18, 2013
09:33Genetic Profiling and Genome-Scale Dropout Screening to Identify Therapeutic Targets in Mouse Models of Malignant Peripheral Nerve Sheath Tumor
Published on: August 25, 2023
Related Concept Videos
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Genomics
Sanger Sequencing