Back to Search
Start Over
Comparison of somatic variant detection algorithms using Ion Torrent targeted deep sequencing data
- Source :
- BMC Medical Genomics, BMC Medical Genomics, Vol 12, Iss S9, Pp 1-11 (2019)
- Publication Year :
- 2019
- Publisher :
- Springer Science and Business Media LLC, 2019.
-
Abstract
- Background The application of next-generation sequencing in cancer has revealed the genomic landscape of many tumour types and is nowadays routinely used in research and clinical settings. Multiple algorithms have been developed to detect somatic variation from sequencing data using either paired tumour-blood or tumour-only samples. Most of these methods have been developed and evaluated for the identification of somatic variation using Illumina sequencing datasets of moderate coverage. However, a comprehensive evaluation of somatic variant detection algorithms on Ion Torrent targeted deep sequencing data has not been performed. Methods We have applied three somatic detection algorithms, Torrent Variant Caller, MuTect2 and VarScan2, on a large cohort of ovarian cancer patients comprising of 208 paired tumour-blood samples and 253 tumour-only samples sequenced deeply on Ion Torrent Proton platform across 330 amplicons. Subsequently, the concordance and performance of the three somatic variant callers were assessed. Results We have observed low concordance across the algorithms with only 0.5% of SNV and 0.02% of INDEL calls in common across all three methods. The intersection of all methods showed better performance when assessed using correlation with known mutational signatures, overlap with COSMIC variation and by examining the variant characteristics. The Torrent Variant Caller also performed well with the advantage of not eliminating a high number of variants that could lead to high type II error. Conclusions Our results suggest that caution should be taken when applying state-of-the-art somatic variant algorithms to Ion Torrent targeted deep sequencing data. Better quality control procedures and strategies that combine results from multiple methods should ensure that higher accuracy is achieved. This is essential to ensure that results from bioinformatics pipelines using Ion Torrent deep sequencing can be robustly applied in cancer research and in the clinic.
- Subjects :
- lcsh:Internal medicine
lcsh:QH426-470
Concordance
Biology
Polymorphism, Single Nucleotide
Somatic variant calling
Deep sequencing
03 medical and health sciences
0302 clinical medicine
Gene Frequency
INDEL Mutation
Ion torrent deep sequencing
Methods evaluation
Genetics
Cancer genome
lcsh:RC31-1245
Indel
Genetics (clinical)
Illumina dye sequencing
030304 developmental biology
0303 health sciences
Research
Genetic Variation
High-Throughput Nucleotide Sequencing
Ion semiconductor sequencing
Amplicon
Read depth
lcsh:Genetics
Mutational signature
030220 oncology & carcinogenesis
DNA microarray
Algorithm
Algorithms
Type I and type II errors
Subjects
Details
- ISSN :
- 17558794
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- BMC Medical Genomics
- Accession number :
- edsair.doi.dedup.....24c327e750d9ccf6579066510297c430
- Full Text :
- https://doi.org/10.1186/s12920-019-0636-y