BAYSIC |
Machine learning (ensemble caller) |
SNV |
Tumor-normal somatic SNV callers |
CaVEMan |
Joint genotype analysis |
SNV |
Tumor-normal somatic SNV callers |
deepSNV |
Allele frequency analysis |
SNV |
Tumor-normal somatic SNV callers |
EBCall |
Allele frequency analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
FaSD-somatic |
Joint genotype analysis |
SNV |
Tumor-normal somatic SNV callers |
FreeBayes |
Haplotype analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
HapMuC |
Haplotype analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
ISOWN |
Supervised learning |
SNV |
Single-sample somatic and germline SNV caller |
JointSNVMix2 |
Joint genotype analysis |
SNV |
Tumor-normal somatic SNV callers |
LocHap |
Haplotype analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
LoFreq |
Allele frequency analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
LoLoPicker |
Allele frequency analysis |
SNV |
Tumor-normal somatic SNV callers |
MutationSeq |
Machine learning |
SNV |
Tumor-normal somatic SNV callers |
MuSE |
Markov chain model |
SNV |
Tumor-normal somatic SNV callers |
MuTect |
Allele frequency analysis |
SNV |
Tumor-normal somatic SNV callers |
OutLyzer |
Noise level estimation |
SNV |
Single-sample somatic and germline SNV caller |
Platypus |
Haplotype analysis |
SNV, indel, sv |
Tumor-normal somatic SNV callers |
Pisces |
Poisson model on read count |
SNV, indel |
Single-sample somatic and germline SNV caller |
PoreSeq |
Nanopore specific |
SNV, indel |
Single-sample somatic and germline SNV caller |
qSNP |
Heuristic threshold |
SNV |
Tumor-normal somatic SNV callers |
RADIA |
Heuristic threshold |
SNV |
Tumor-normal somatic SNV callers |
Seurat |
Joint genotype analysis |
SNV, indel,sv |
Tumor-normal somatic SNV callers |
SAMtools |
Joint genotype analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
Shimmer |
Heuristic threshold |
SNV, indel |
Tumor-normal somatic SNV callers |
SNooPer |
Machine learning |
SNV, indel |
Tumor-normal somatic SNV callers |
SNVSniffer |
Joint genotype analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
SOAPsnv |
Heuristic threshold |
SNV |
Tumor-normal somatic SNV callers |
SomaticSeq |
Machine learning (ensemble caller) |
SNV |
Tumor-normal somatic SNV callers |
SomaticSniper |
Joint genotype analysis |
SNV |
Tumor-normal somatic SNV callers |
Strelka |
Allele frequency analysis |
SNV, indel |
Tumor-normal somatic SNV callers |
Shearwater |
Noise level estimation |
SNV |
Single-sample somatic and germline SNV caller |
SiNVICT |
Poisson model on read count |
SNV, indel |
Single-sample somatic and germline SNV caller |
SNVer |
Allele frequency analysis |
SNV, indel |
Single-sample somatic and germline SNV caller |
SNVMix2 |
Genotype analysis |
SNV |
Single-sample somatic and germline SNV caller |
SomVarIUS |
Noise level estimation |
SNV, indel |
Single-sample somatic and germline SNV caller |
SPLINTER |
Noise level estimation |
SNV, indel |
Single-sample somatic and germline SNV caller |
TVC |
Ion Torrent specific |
SNV, indel, SV |
Tumor-normal somatic SNV callers |
VarDict |
Heuristic threshold |
SNV, indel, SV |
Tumor-normal somatic SNV callers |
VarScan2 |
Heuristic threshold |
SNV, indel |
Tumor-normal somatic SNV callers |
Virmid |
Joint genotype analysis |
SNV |
Tumor-normal somatic SNV callers |